Conocer tu predisposición genética a padecer enfermedades comunes, crónicas y que pueden ser tratadas con fármacos, puede ayudarte a prevenirlas.
Secuenciación de exomas
EXOMAS
Alport, síndrome
Ref. 4693
3 genes
- COL4A3
- COL4A4
- COL4A5
EXOMAS
Alzheimer, enfermedad
Ref. 3659
9 genes
- A2M
- APOE
- APP
- HFE
- MPO
- NOS3
- PLAU
- PSEN1
- PSEN2
EXOMAS
Amiloidosis Familiar
Ref. 3985
17 genes
- APOA1
- APOA2
- APP
- B2M
- CST3
- FGA
- GPNMB
- GSN
- IL31RA
- ITM2B
- LYZ
- MEFV
- NLRP3
- OSMR
- PRNP
- TNFRSF1A
- TTR
EXOMAS
Ataxia Episódica
Ref. 3663
6 genes
- ATP1A3
- CACNA1A
- CACNB4
- KCNA1
- SCN2A
- SLC1A3
EXOMAS
Beckwith-Wiedemann, síndrome
Ref. 4199
8 genes
- CDKN1C
- DIS3L2
- GPC3
- GPC4
- HRAS
- IGF2
- KCNQ1
- NSD1
EXOMAS
Cáncer Gástrico Hereditario
Ref. 3896
15 genes
- APC
- ATM
- BMPR1A
- BRCA1
- BRCA2
- CDH1
- EPCAM
- MLH1
- MSH2
- MSH6
- PMS2
- PTEN
- SMAD4
- STK11
- TP53
EXOMAS
Cavernomatosis Múltiple
Ref. 3988
3 genes
- CCM2
- KRIT1
- PDCD10
EXOMAS
Disgenesia Gonadal (46,XY)
Ref. 4717
12 genes
- AKR1C2
- AKR1C4
- ARX
- CBX2
- DHCR7
- DHH
- MAP3K1
- NR0B1
- NR5A1
- SOX9
- SRY
- ZFPM2
EXOMAS
Disgenesia Gonadal (46,XY)
Ref. 3780
9 genes
- AKR1C2
- AKR1C4
- CBX2
- DHH
- MAP3K1
- NR0B1
- NR5A1
- SRY
- ZFPM2
EXOMAS
Displasia Arritmogénica del Ventrículo Derecho
Ref. 4277
13 genes
- CTNNA3
- DES
- DSC2
- DSG2
- DSP
- JUP
- LMNA
- PKP2
- PLN
- RYR2
- TGFB3
- TMEM43
- TTN
EXOMAS
Displasia Epifisaria Múltiple
Ref. 3687
7 genes
- CANT1
- COL9A1
- COL9A2
- COL9A3
- COMP
- MATN3
- SLC26A2
EXOMAS
Gorlin, síndrome
Ref. 4028
3 genes
- PTCH1
- PTCH2
- SUFU
EXOMAS
Hemocromatosis
Ref. 3765
7 genes
- BMP2
- FTH1
- HAMP
- HFE
- HJV
- SLC40A1
- TFR2
EXOMAS
Ictiosis Congénita
Ref. 3968
14 genes
- ABCA12
- ALOX12B
- ALOXE3
- CASP14
- CERS3
- CYP4F22
- LIPN
- NIPAL4
- PNPLA1
- SDR9C7
- SLC27A4
- ST14
- SULT2B1
- TGM1
EXOMAS
Leigh, síndrome
Ref. 3698
69 genes
- AIFM1
- BCS1L
- BTD
- C12orf65
- COX10
- COX15
- COX8A
- DLAT
- DLD
- EARS2
- ECHS1
- ETHE1
- FARS2
- FBXL4
- FOXRED1
- GFM1
- GFM2
- GTPBP3
- HIBCH
- IARS2
- LIAS
- LIPT1
- LRPPRC
- MTFMT
- NARS2
- NDUFA1
- NDUFA10
- NDUFA11
- NDUFA12
- NDUFA2
- NDUFA4
- NDUFA9
- NDUFAF2
- NDUFAF3
- NDUFAF4
- NDUFAF5
- NDUFAF6
- NDUFAF8
- NDUFS1
- NDUFS2
- NDUFS3
- NDUFS4
- NDUFS7
- NDUFS8
- NDUFV1
- NDUFV2
- NUBPL
- PDHA1
- PDHB
- PDHX
- PDSS2
- PET100
- PNPT1
- POLG
- SCO2
- SDHA
- SDHAF1
- SERAC1
- SLC19A3
- SLC25A19
- SUCLA2
- SUCLG1
- SURF1
- TACO1
- TPK1
- TRMU
- TSFM
- TTC19
- UQCRQ
EXOMAS
Marfan, síndrome
Ref. 3772
18 genes
- CBS
- COL11A1
- COL11A2
- COL2A1
- COL3A1
- COL5A1
- COL5A2
- COL9A1
- COL9A2
- COL9A3
- FBN1
- FBN2
- PLOD1
- SMAD3
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
EXOMAS
Melanoma Hereditario
Ref. 3894
2 genes
- CDK4
- CDKN2A
EXOMAS
Miocardiopatía Dilatada
Ref. 4278
55 genes
- ABCC9
- ACTC1
- ACTN2
- ANKRD1
- BAG3
- CAV3
- CRYAB
- CSRP3
- DES
- DMD
- DSC2
- DSG2
- DSP
- EMD
- EYA4
- FHL1
- FHL2
- FKRP
- FKTN
- GATAD1
- HFE
- ILK
- JUP
- LAMA4
- LAMP2
- LDB3
- LMNA
- MYBPC3
- MYH6
- MYH7
- MYPN
- NEXN
- PDLIM3
- PKP2
- PLN
- PRDM16
- PSEN1
- PSEN2
- RAF1
- RBM20
- RYR2
- SCN5A
- SDHA
- SGCD
- TAZ
- TBX20
- TCAP
- TMPO
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TTN
- TXNRD2
- VCL
EXOMAS
Miocardiopatía Hipertrófica
Ref. 4279
53 genes
- ACTC1
- ACTN2
- ALPK3
- ANKRD1
- BRAF
- CALR3
- CAV3
- CSRP3
- FLNC
- FXN
- GAA
- GLA
- HRAS
- JPH2
- KLF10
- KRAS
- LAMP2
- LDB3
- LZTR1
- MAP2K1
- MAP2K2
- MYBPC3
- MYH6
- MYH7
- MYL2
- MYL3
- MYLK2
- MYOM1
- MYOZ2
- MYPN
- NEXN
- NRAS
- OBSCN
- PDLIM3
- PLN
- PRKAG2
- PTPN11
- RAF1
- RASA2
- RIT1
- RRAS
- RYR2
- SOS1
- SOS2
- TCAP
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TRIM63
- TTN
- TTR
- VCL
EXOMAS
Miocardiopatía Hipertrófica
Ref. 3549
31 genes
- ACTC1
- ACTN2
- CALR3
- CAV3
- CSRP3
- DES
- FLNC
- GLA
- JPH2
- LAMP2
- LDB3
- MYBPC3
- MYH6
- MYH7
- MYL2
- MYL3
- MYLK2
- MYOZ2
- MYPN
- NEXN
- PLN
- PRKAG2
- PTPN11
- TCAP
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TTN
- TTR
- VCL
EXOMAS
Tumor de Wilms
Ref. 4195
16 genes
- BLM
- BRCA2
- BUB1B
- CDC73
- CTR9
- DICER1
- DIS3L2
- GPC3
- GPC4
- PALB2
- PIK3CA
- POU6F2
- REST
- TP53
- TRIM37
- WT1
EXOMAS
Noonan, síndrome
Ref. 4083
18 genes
- A2ML1
- BRAF
- HRAS
- KRAS
- LZTR1
- MAP2K1
- MAP2K2
- NF1
- NRAS
- PTPN11
- RAF1
- RASA2
- RIT1
- RRAS
- SHOC2
- SOS1
- SOS2
- SPRED1
EXOMAS
Osteogénesis Imperfecta
Ref. 4760
18 genes
- BMP1
- COL1A1
- COL1A2
- CREB3L1
- CRTAP
- FKBP10
- IFITM5
- MBTPS2
- MESD
- P3H1
- PPIB
- SERPINF1
- SERPINH1
- SP7
- SPARC
- TENT5A
- TMEM38B
- WNT1
EXOMAS
Osteogénesis Imperfecta
Ref. 4040
17 genes
- BMP1
- COL1A1
- COL1A2
- CREB3L1
- CRTAP
- FKBP10
- IFITM5
- MBTPS2
- P3H1
- PPIB
- SERPINF1
- SERPINH1
- SP7
- SPARC
- TENT5A
- TMEM38B
- WNT1
EXOMAS
Osteogénesis Imperfecta
Ref. 4084
12 genes
- BMP1
- COL1A1
- COL1A2
- CRTAP
- FKBP10
- IFITM5
- P3H1
- PLOD2
- PPIB
- SERPINF1
- SERPINH1
- SP7
EXOMAS
Pancreatitis Hereditaria
Ref. 4104
4 genes
- CFTR
- CTRC
- PRSS1
- SPINK1
EXOMAS
Feocromocitoma-paraganglioma hereditario
Ref. 3899
12 genes
- FH
- KIF1B
- MAX
- NF1
- RET
- SDHA
- SDHAF2
- SDHB
- SDHC
- SDHD
- TMEM127
- VHL
EXOMAS
Feocromocitoma-paraganglioma hereditario
Ref. 4080
11 genes
- MAX
- MEN1
- NF1
- RET
- SDHA
- SDHAF2
- SDHB
- SDHC
- SDHD
- TMEM127
- VHL
EXOMAS
Poliposis Adenomatosa Familiar
Ref. 4773
5 genes
- APC
- BMPR1A
- MUTYH
- NTHL1
- SMAD4
EXOMAS
QT largo, síndrome
Ref. 10008
18 genes
- AKAP9
- ALG10B
- ANK2
- CACNA1C
- CALM1
- CALM2
- CALM3
- CAV3
- KCNE1
- KCNE2
- KCNH2
- KCNJ2
- KCNJ5
- KCNQ1
- RYR2
- SCN4B
- SCN5A
- SNTA1
EXOMAS
QT largo, síndrome
Ref. 3544
17 genes
- AKAP9
- ALG10
- ANK2
- CACNA1C
- CALM1
- CALM2
- CAV3
- KCNE1
- KCNE2
- KCNH2
- KCNJ2
- KCNJ5
- KCNQ1
- RYR2
- SCN4B
- SCN5A
- SNTA1
EXOMAS
QT largo, síndrome
Ref. 4256
17 genes
- AKAP9
- ALG10B
- ANK2
- CACNA1C
- CALM1
- CALM2
- CAV3
- KCNE1
- KCNE2
- KCNH2
- KCNJ2
- KCNJ5
- KCNQ1
- RYR2
- SCN4B
- SCN5A
- SNTA1
EXOMAS
Retinoblastoma hereditario
Ref. 3900
1 genes
- RB1
EXOMAS
Sotos, síndrome
Ref. 4689
3 genes
- APC2
- NFIX
- NSD1
EXOMAS
Brugada, síndrome
Ref. 4076
25 genes
- ABCC9
- ANK2
- ANK3
- CACNA1C
- CACNA1D
- CACNA2D1
- CACNB2
- FGF12
- GPD1L
- HCN4
- KCND2
- KCND3
- KCNE3
- KCNE5
- KCNH2
- KCNJ8
- PKP2
- RANGRF
- SCN10A
- SCN1B
- SCN2B
- SCN3B
- SCN5A
- SLMAP
- TRPM4
EXOMAS
Brugada, síndrome
Ref. 3550
23 genes
- ABCC9
- CACNA1C
- CACNA2D1
- CACNB2
- FGF12
- GPD1L
- HCN4
- KCND2
- KCND3
- KCNE3
- KCNE5
- KCNH2
- KCNJ8
- PKP2
- RANGRF
- SCN10A
- SCN1B
- SCN2B
- SCN3B
- SCN5A
- SEMA3A
- SLMAP
- TRPM4
EXOMAS
Encefalopatía de Sustancia Blanca Evanescente
Ref. 4001
5 genes
- EIF2B1
- EIF2B2
- EIF2B3
- EIF2B4
- EIF2B5
EXOMAS
Defecto Congénito de la Glicosilación
Ref. 3710
43 genes
- ALG1
- ALG11
- ALG12
- ALG13
- ALG2
- ALG3
- ALG6
- ALG8
- ALG9
- ATP6V0A2
- B4GALT1
- CCDC115
- COG1
- COG2
- COG4
- COG5
- COG6
- COG7
- COG8
- DDOST
- DOLK
- DPAGT1
- DPM1
- DPM2
- DPM3
- MGAT2
- MOGS
- MPDU1
- MPI
- NUS1
- PGM1
- PMM2
- RFT1
- SLC35A1
- SLC35A2
- SLC35C1
- SLC39A8
- SRD5A3
- SSR4
- STT3A
- STT3B
- TMEM165
- TMEM199
EXOMAS
Rubinstein-Taybi, síndrome
Ref. 4681
2 genes
- CREBBP
- EP300
EXOMAS
Bardet-Biedl, síndrome
Ref. 3600
23 genes
- ARL6
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- C8orf37
- CCDC28B
- CEP290
- IFT27
- IFT74
- LZTFL1
- MKKS
- MKS1
- SDCCAG8
- TMEM67
- TRIM32
- TTC8
- WDPCP
EXOMAS
Glomeruloesclerosis Focal y Segmentaria
Ref. 3655
9 genes
- ACTN4
- ANLN
- APOL1
- CD2AP
- CRB2
- INF2
- MYO1E
- PAX2
- TRPC6
EXOMAS
Stickler, síndrome
Ref. 4531
5 genes
- COL11A1
- COL11A2
- COL2A1
- COL9A1
- COL9A2
EXOMAS
Stickler, síndrome
Ref. 3750
6 genes
- COL11A1
- COL11A2
- COL2A1
- COL9A1
- COL9A2
- COL9A3
EXOMAS
Lynch, síndrome
Ref. 4770
7 genes
- EPCAM
- MLH1
- MLH3
- MSH2
- MSH3
- MSH6
- PMS2
EXOMAS
Cornelia de Lange, síndrome
Ref. 4662
10 genes
- ANKRD11
- BRD4
- HDAC8
- NIPBL
- PACS1
- RAD21
- SMC1A
- SMC3
- STAG1
- STAG2
EXOMAS
Cornelia de Lange, síndrome
Ref. 3886
7 genes
- ANKRD11
- BRD4
- HDAC8
- NIPBL
- RAD21
- SMC1A
- SMC3
EXOMAS
Hipogonadismo Hipogonadotrópico
Ref. 4762
25 genes
- ANOS1
- CHD7
- DUSP6
- FEZF1
- FGF17
- FGF8
- FGFR1
- FLRT3
- FSHB
- GNRH1
- GNRHR
- HS6ST1
- IL17RD
- KISS1
- KISS1R
- LHB
- NDNF
- NSMF
- PROK2
- PROKR2
- SEMA3A
- SPRY4
- TAC3
- TACR3
- WDR11
EXOMAS
Hipogonadismo Hipogonadotrópico
Ref. 3771
24 genes
- ANOS1
- CHD7
- DUSP6
- FEZF1
- FGF17
- FGF8
- FGFR1
- FLRT3
- FSHB
- GNRH1
- GNRHR
- HS6ST1
- IL17RD
- KISS1
- KISS1R
- LHB
- NSMF
- PROK2
- PROKR2
- SEMA3A
- SPRY4
- TAC3
- TACR3
- WDR11
EXOMAS
Hipertensión Pulmonar Primaria
Ref. 4007
4 genes
- BMPR2
- CAV1
- KCNK3
- SMAD9
EXOMAS
Bannayan-Riley-Ruvalcaba/Cowden, síndrome
Ref. 10066
15 genes
- AKT1
- BMPR1A
- FLCN
- KLLN
- NF1
- PIK3CA
- PTCH1
- PTEN
- SDHB
- SDHC
- SDHD
- SEC23B
- SMAD4
- STK11
- SUFU
EXOMAS
Bannayan-Riley-Ruvalcaba/Cowden, síndrome
Ref. 3760
7 genes
- AKT1
- KLLN
- PIK3CA
- PTEN
- SDHB
- SDHD
- SEC23B
EXOMAS
Epilepsia Generalizada con Crisis Febriles Plus (GEFS )
Ref. 4266
7 genes
- GABRD
- GABRG2
- HCN1
- SCN1A
- SCN1B
- SCN9A
- STX1B
EXOMAS
Robinow, síndrome
Ref. 4337
5 genes
- DVL1
- DVL3
- NXN
- ROR2
- WNT5A
EXOMAS
Stargardt, síndrome
Ref. 3636
3 genes
- ABCA4
- ELOVL4
- PROM1
EXOMAS
Neurodegeneración con acumulación cerebral de hierro
Ref. 4646
22 genes
- ATP13A2
- C19orf12
- COASY
- CP
- CRAT
- DCAF17
- FA2H
- FTL
- FUCA1
- GCDH
- KIF1A
- KMT2B
- PANK2
- PLA2G6
- PSEN1
- REPS1
- SCP2
- SLC39A14
- SQSTM1
- UBTF
- VPS13A
- WDR45
EXOMAS
Anemia de Fanconi
Ref. 3967
21 genes
- BRCA1
- BRCA2
- BRIP1
- ERCC4
- FANCA
- FANCB
- FANCC
- FANCD2
- FANCE
- FANCF
- FANCG
- FANCI
- FANCL
- MAD2L2
- PALB2
- RAD51
- RAD51C
- RFWD3
- SLX4
- UBE2T
- XRCC2
EXOMAS
Ondine , síndrome
Ref. 3773
6 genes
- ASCL1
- BDNF
- EDN3
- GDNF
- PHOX2B
- RET
EXOMAS
Nefrótico, síndrome
Ref. 4046
60 genes
- ACTN4
- ALG1
- ANLN
- APOL1
- ARHGAP24
- ARHGDIA
- CD151
- CD2AP
- CFH
- COL4A3
- COL4A4
- COL4A5
- COQ2
- COQ6
- COQ8B
- CRB2
- CUBN
- DGKE
- E2F3
- EMP2
- FAT1
- GPC5
- INF2
- ITGA3
- ITGB4
- KANK1
- KANK2
- KANK4
- LAMB2
- LMNA
- LMX1B
- MAGI2
- MYH9
- MYO1E
- NPHS1
- NPHS2
- NUP107
- NUP133
- NUP160
- NUP205
- NUP85
- NUP93
- NXF5
- OCRL
- PAX2
- PDSS2
- PLCE1
- PMM2
- PODXL
- PTPRO
- SCARB2
- SGPL1
- SMARCAL1
- SYNPO
- TRPC6
- TTC21B
- WDR73
- WT1
- XPO5
- ZMPSTE24
EXOMAS
Klippel-Feil, síndrome
Ref. 4730
4 genes
- GDF3
- GDF6
- MEOX1
- MYO18B
EXOMAS
Migraña Hemipléjica Familiar
Ref. 4008
16 genes
- ACVRL1
- AMACR
- ATP1A2
- CACNA1A
- ENG
- NOTCH3
- PDGFB
- PEX11B
- PGK1
- PRRT2
- SCN1A
- SLC1A3
- SLC2A1
- STIM1
- TNF
- TREX1
EXOMAS
Acromatopsia
Ref. 4685
10 genes
- ATF6
- CNGA3
- CNGB3
- CNNM4
- GNAT2
- OPN1LW
- OPN1MW
- OPN1SW
- PDE6C
- PDE6H
EXOMAS
Acromatopsia
Ref. 3983
6 genes
- ATF6
- CNGA3
- CNGB3
- GNAT2
- PDE6C
- PDE6H
EXOMAS
Amaurosis Congénita de Leber
Ref. 10055
27 genes
- AIPL1
- ALMS1
- CABP4
- CEP290
- CLUAP1
- CRB1
- CRX
- DTHD1
- GDF6
- GUCY2D
- IFT140
- IMPDH1
- IQCB1
- KCNJ13
- LCA5
- LRAT
- NMNAT1
- OTX2
- PRPH2
- RD3
- RDH12
- ROM1
- RPE65
- RPGRIP1
- SPATA7
- TULP1
- USP45
EXOMAS
Amaurosis Congénita de Leber
Ref. 4287
26 genes
- AIPL1
- ALMS1
- CABP4
- CEP290
- CLUAP1
- CRB1
- CRX
- DTHD1
- GDF6
- GUCY2D
- IFT140
- IMPDH1
- IQCB1
- KCNJ13
- LCA5
- LRAT
- NMNAT1
- OTX2
- PRPH2
- RD3
- RDH12
- ROM1
- RPE65
- RPGRIP1
- SPATA7
- TULP1
EXOMAS
Seckel, síndrome
Ref. 3692
9 genes
- ATR
- CENPJ
- CEP152
- CEP63
- DNA2
- NIN
- NSMCE2
- RBBP8
- TRAIP
EXOMAS
Kabuki, síndrome
Ref. 4765
2 genes
- KDM6A
- KMT2D
EXOMAS
Hiperekplexia o síndrome del Sobresalto Exagerado
Ref. 3844
5 genes
- ARHGEF9
- GLRA1
- GLRB
- GPHN
- SLC6A5
EXOMAS
Dishormonogénesis tiroidea familiar
Ref. 3997
7 genes
- DUOX2
- DUOXA2
- IYD
- SLC26A4
- SLC5A5
- TG
- TPO
EXOMAS
Esferocitosis hereditaria
Ref. 3789
5 genes
- ANK1
- EPB42
- SLC4A1
- SPTA1
- SPTB
EXOMAS
Miastenia Congénita
Ref. 4039
24 genes
- AGRN
- ALG14
- ALG2
- CHAT
- CHRNA1
- CHRNB1
- CHRND
- CHRNE
- COL13A1
- COLQ
- DOK7
- DPAGT1
- GFPT1
- LRP4
- MUSK
- MYO9A
- PREPL
- RAPSN
- SCN4A
- SLC18A3
- SLC25A1
- SLC5A7
- SNAP25
- SYT2
EXOMAS
Miopatía Nemalínica
Ref. 3678
11 genes
- ACTA1
- CFL2
- KBTBD13
- KLHL40
- KLHL41
- LMOD3
- MYPN
- NEB
- TNNT1
- TPM2
- TPM3
EXOMAS
Disquinesia Ciliar Primaria
Ref. 4721
47 genes
- ARMC4
- CCDC103
- CCDC114
- CCDC151
- CCDC39
- CCDC40
- CCDC65
- CCNO
- CFAP221
- CFAP298
- CFAP300
- DNAAF1
- DNAAF2
- DNAAF3
- DNAAF4
- DNAAF5
- DNAH1
- DNAH11
- DNAH5
- DNAH8
- DNAH9
- DNAI1
- DNAI2
- DNAJB13
- DNAL1
- DRC1
- FOXJ1
- GAS2L2
- GAS8
- HYDIN
- LRRC56
- LRRC6
- MCIDAS
- NEK10
- NME8
- OFD1
- PIH1D3
- RSPH1
- RSPH3
- RSPH4A
- RSPH9
- SPAG1
- SPEF2
- STK36
- TTC12
- TTC25
- ZMYND10
EXOMAS
Linfedema congénito
Ref. 4563
5 genes
- EPHB4
- FLT4
- GJC2
- PIEZO1
- VEGFC
EXOMAS
Déficit de surfactante pulmonar
Ref. 4555
7 genes
- ABCA3
- CSF2RA
- CSF2RB
- FOXF1
- NKX2-1
- SFTPB
- SFTPC
EXOMAS
Cáncer de Próstata Hereditario
Ref. 3897
14 genes
- ABRAXAS1
- ATM
- BRCA1
- BRCA2
- BRIP1
- CHEK2
- MRE11
- MSH2
- MSH6
- NBN
- PALB2
- PMS2
- RAD51C
- RAD51D
EXOMAS
Enfermedades Mitocondriales
Ref. 3665
357 genes
- AARS2
- AASS
- ABAT
- ABCB6
- ABCB7
- ABCD1
- ACACA
- ACAD8
- ACAD9
- ACADL
- ACADM
- ACADS
- ACADSB
- ACADVL
- ACAT1
- ACO2
- ACOX1
- ACSF3
- ACSL4
- AFG3L2
- AGK
- AGXT
- AIFM1
- AK2
- ALAS2
- ALDH18A1
- ALDH2
- ALDH3A2
- ALDH4A1
- ALDH5A1
- ALDH6A1
- ALDH7A1
- AMACR
- AMT
- APOPT1
- ARMS2
- ASS1
- ATIC
- ATP5F1A
- ATP5F1E
- ATP7B
- ATPAF2
- AUH
- BAX
- BCKDHA
- BCKDHB
- BCKDK
- BCL2
- BCS1L
- BOLA3
- BTD
- C12orf65
- CA5A
- CARS2
- CASP8
- CAT
- CAVIN1
- CHCHD10
- CISD2
- CLN3
- CLPB
- CLPP
- COA5
- COA6
- COASY
- COQ2
- COQ4
- COQ6
- COQ7
- COQ8A
- COQ8B
- COQ9
- COX10
- COX14
- COX15
- COX20
- COX4I2
- COX6A1
- COX6B1
- COX7B
- COX8A
- CPOX
- CPS1
- CPT1A
- CPT1C
- CPT2
- CYB5A
- CYB5R3
- CYBB
- CYC1
- CYCS
- CYP11A1
- CYP11B1
- CYP11B2
- CYP24A1
- CYP27A1
- CYP27B1
- D2HGDH
- DARS2
- DBT
- DECR1
- DGUOK
- DHODH
- DHTKD1
- DIABLO
- DLAT
- DLD
- DMGDH
- DMPK
- DNA2
- DNAJC19
- DNM1L
- DNM2
- EARS2
- ECHS1
- EHHADH
- ELAC2
- ETFA
- ETFB
- ETFDH
- ETHE1
- FARS2
- FASTKD2
- FBXL4
- FECH
- FH
- FOXRED1
- FXN
- GARS
- GATM
- GCDH
- GCK
- GCSH
- GDAP1
- GFER
- GFM1
- GFM2
- GK
- GLDC
- GLRX5
- GLUD1
- GLYCTK
- GPD2
- GPT2
- GPX1
- GSR
- GTPBP3
- HADH
- HADHA
- HADHB
- HARS2
- HAX1
- HCCS
- HIBCH
- HK1
- HLCS
- HMGCL
- HMGCS2
- HOGA1
- HSD17B10
- HSD3B2
- HSPA9
- HSPD1
- HTRA2
- IARS2
- IBA57
- IDH2
- IDH3B
- ISCA2
- ISCU
- IVD
- KARS
- KIF1B
- L2HGDH
- LARS2
- LIAS
- LIPT1
- LONP1
- LRPPRC
- LYRM4
- LYRM7
- MAOA
- MAOB
- MARS2
- MCCC1
- MCCC2
- MCEE
- MFN2
- MGME1
- MICU1
- MLYCD
- MMAA
- MMAB
- MMACHC
- MMADHC
- MOCS1
- MPC1
- MPV17
- MRPL3
- MRPL44
- MRPS16
- MRPS22
- MSRB3
- MTFMT
- MTHFD1
- MTO1
- MTPAP
- MTRR
- MUT
- MUTYH
- NADK2
- NAGS
- NARS2
- NDUFA1
- NDUFA10
- NDUFA11
- NDUFA12
- NDUFA13
- NDUFA2
- NDUFA4
- NDUFA9
- NDUFAF1
- NDUFAF2
- NDUFAF3
- NDUFAF4
- NDUFAF5
- NDUFAF6
- NDUFB11
- NDUFB3
- NDUFB9
- NDUFS1
- NDUFS2
- NDUFS3
- NDUFS4
- NDUFS6
- NDUFS7
- NDUFS8
- NDUFV1
- NDUFV2
- NFU1
- NNT
- NTHL1
- NUBPL
- OAT
- OGDH
- OGG1
- OPA1
- OPA3
- OTC
- OXCT1
- PAM16
- PANK2
- PARK7
- PC
- PCCA
- PCCB
- PCK2
- PDHA1
- PDHB
- PDHX
- PDK3
- PDP1
- PDSS1
- PDSS2
- PDX1
- PET100
- PHB
- PINK1
- PNKD
- PNPT1
- POLG
- POLG2
- PPM1K
- PPOX
- PRODH
- PTRH2
- PTS
- PUS1
- PYCR1
- PYCR2
- QDPR
- RARS2
- REEP1
- RMND1
- RNASEL
- RRM2B
- SARDH
- SARS2
- SCO1
- SCO2
- SCP2
- SDHA
- SDHAF1
- SDHAF2
- SDHB
- SDHC
- SDHD
- SERAC1
- SFXN4
- SLC16A1
- SLC19A3
- SLC25A1
- SLC25A12
- SLC25A13
- SLC25A15
- SLC25A19
- SLC25A20
- SLC25A22
- SLC25A3
- SLC25A38
- SLC25A4
- SLC25A46
- SOD1
- SOD2
- SPART
- SPG7
- SPTLC2
- STAR
- STOM
- SUCLA2
- SUCLG1
- SUGCT
- SUOX
- SURF1
- TACO1
- TARS2
- TAZ
- TCIRG1
- TIMM44
- TIMM8A
- TK2
- TMEM126A
- TMEM70
- TMLHE
- TPP1
- TRMU
- TRNT1
- TSFM
- TTBK2
- TTC19
- TUFM
- TWNK
- TXNRD2
- TYMP
- UCP1
- UCP3
- UNG
- UQCC2
- UQCRB
- UQCRC2
- UQCRQ
- UROS
- VARS2
- WARS2
- WDR81
- XPNPEP3
- YARS2
EXOMAS
Lisencefalia
Ref. 4542
25 genes
- ACTB
- ACTG1
- ADGRG1
- ARX
- CDK5
- DCX
- DYNC1H1
- FKRP
- FKTN
- KATNB1
- KIF2A
- LAMB1
- LARGE1
- MACF1
- NDE1
- PAFAH1B1
- POMGNT1
- POMT1
- POMT2
- RELN
- TMTC3
- TUBA1A
- TUBB2B
- TUBG1
- VLDLR
EXOMAS
Displasias esqueléticas
Ref. 3871
254 genes
- ACAN
- ACP5
- ACVR1
- ADAMTSL2
- AGA
- AGPS
- AKT1
- ALPL
- ALX1
- ALX3
- ALX4
- AMER1
- ANKH
- ANO5
- ANTXR2
- ARHGAP31
- ARSB
- ARSE
- ATP6V0A2
- B3GALT6
- B4GALT7
- BMP1
- BMP2
- BMPER
- BMPR1B
- CA2
- CANT1
- CASR
- CC2D2A
- CCNQ
- CDH3
- CDKN1C
- CEP290
- CHST14
- CHST3
- CHSY1
- CLCN5
- CLCN7
- COG1
- COL10A1
- COL11A1
- COL11A2
- COL1A1
- COL1A2
- COL2A1
- COL9A1
- COL9A2
- COL9A3
- COMP
- CREBBP
- CRTAP
- CTSA
- CTSK
- CUL7
- DDR2
- DHCR24
- DHODH
- DLL3
- DLX3
- DMP1
- DYM
- DYNC2H1
- EBP
- EFNB1
- EIF2AK3
- ENPP1
- EP300
- ESCO2
- EVC
- EVC2
- EXT1
- EXT2
- EZH2
- FAM111A
- FAM20C
- FBLN1
- FBN1
- FBXW4
- FERMT3
- FGF10
- FGF23
- FGF9
- FGFR1
- FGFR2
- FGFR3
- FIG4
- FKBP10
- FLNA
- FLNB
- FMN1
- FUCA1
- GALNS
- GALNT3
- GDF5
- GDF6
- GJA1
- GLB1
- GLI3
- GNAS
- GNPAT
- GNPTAB
- GNPTG
- GNS
- GORAB
- GPC6
- GREM1
- GUSB
- HDAC4
- HES7
- HGSNAT
- HOXA11
- HOXA13
- HOXD13
- HPGD
- HSPG2
- ICK
- IDS
- IDUA
- IFITM5
- IFT122
- IFT140
- IFT80
- IHH
- IKBKG
- IL1RN
- INPPL1
- KAT6B
- KIF22
- KIF7
- LBR
- LEMD3
- LFNG
- LIFR
- LMBR1
- LMNA
- LMX1B
- LPIN2
- LRP4
- LRP5
- LTBP3
- MAFB
- MAN2B1
- MANBA
- MATN3
- MESP2
- MGP
- MKS1
- MMP13
- MMP2
- MMP9
- MNX1
- MSX2
- MYCN
- NAGLU
- NEK1
- NEU1
- NF1
- NFIX
- NIPBL
- NKX3-2
- NLRP3
- NME1
- NOG
- NOTCH2
- NPPC
- NPR2
- NSD1
- NSDHL
- OBSL1
- OFD1
- ORC1
- OSTM1
- P3H1
- PAPSS2
- PCNT
- PCYT1A
- PDE4D
- PEX7
- PHEX
- PIGV
- PITX1
- PLEKHM1
- PLOD2
- POLR1C
- POLR1D
- POR
- PPIB
- PRKAR1A
- PTH1R
- PTHLH
- PTPN11
- PYCR1
- RAB23
- RASGRP2
- RECQL4
- ROR2
- RPGRIP1L
- RUNX2
- SALL1
- SALL4
- SBDS
- SERPINF1
- SERPINH1
- SF3B4
- SGSH
- SH3BP2
- SH3PXD2B
- SHH
- SHOX
- SKI
- SLC17A5
- SLC26A2
- SLC34A3
- SLC35D1
- SLC39A13
- SMARCAL1
- SOST
- SOX9
- SP7
- SUMF1
- TBCE
- TBX15
- TBX3
- TBX4
- TBX5
- TBXAS1
- TCIRG1
- TCOF1
- TCTN3
- TGFB1
- TGFBR1
- TGFBR2
- THPO
- TMEM216
- TMEM38B
- TMEM67
- TNFRSF11A
- TNFRSF11B
- TNFSF11
- TP63
- TRAPPC2
- TREM2
- TRIP11
- TRPS1
- TRPV4
- TTC21B
- TWIST1
- TYROBP
- WDR35
- WISP3
- WNT3
- WNT5A
- WNT7A
- ZMPSTE24
EXOMAS
Glaucoma hereditario
Ref. 4003
9 genes
- ASB10
- CYP1B1
- LTBP2
- MYOC
- NTF4
- OPTN
- TBK1
- TEK
- WDR36
EXOMAS
Convulsiones neonatales-infantiles benignas familiares
Ref. 3991
3 genes
- PRRT2
- SCN2A
- SCN8A
EXOMAS
Jarabe de arce, enfermedad
Ref. 3842
5 genes
- BCKDHA
- BCKDHB
- DBT
- DLD
- PPM1K
EXOMAS
Xeroderma Pigmentoso
Ref. 4139
9 genes
- DDB2
- ERCC1
- ERCC2
- ERCC3
- ERCC4
- ERCC5
- POLH
- XPA
- XPC
EXOMAS
Cockayne, síndrome
Ref. 3989
5 genes
- ERCC3
- ERCC4
- ERCC5
- ERCC6
- ERCC8
EXOMAS
Holoprosencefalia
Ref. 3790
14 genes
- CDON
- DISP1
- DLL1
- FGF8
- FOXH1
- GAS1
- GLI2
- NODAL
- PTCH1
- SHH
- SIX3
- TDGF1
- TGIF1
- ZIC2
EXOMAS
Encefalopatía epiléptica infantil temprana
Ref. 4264
77 genes
- AARS
- ACTL6B
- ADAM22
- ALG13
- AP3B2
- ARHGEF9
- ARV1
- ARX
- CACNA1A
- CACNA1E
- CAD
- CDKL5
- CNPY3
- CPLX1
- CUX2
- CYFIP2
- DENND5A
- DNM1
- DOCK7
- EEF1A2
- FGF12
- FRRS1L
- GABBR2
- GABRA1
- GABRB1
- GABRB3
- GABRG2
- GLS
- GNAO1
- GRIN2B
- GRIN2D
- GUF1
- HCN1
- HNRNPU
- ITPA
- KCNA2
- KCNB1
- KCNQ2
- KCNT1
- KCNT2
- MDH2
- NECAP1
- NEUROD2
- NTRK2
- PACS2
- PARS2
- PCDH19
- PHACTR1
- PIGA
- PIGP
- PLCB1
- PNKP
- RHOBTB2
- RNF13
- SCN1A
- SCN1B
- SCN2A
- SCN3A
- SCN8A
- SCN9A
- SIK1
- SLC12A5
- SLC13A5
- SLC1A2
- SLC25A12
- SLC25A22
- SLC35A2
- SPTAN1
- ST3GAL3
- STXBP1
- SYNJ1
- SZT2
- TBC1D24
- TRAK1
- UBA5
- WWOX
- YWHAG
EXOMAS
Encefalopatía epiléptica infantil temprana
Ref. 4502
200 genes
- ABAT
- ADAM22
- ADSL
- ALDH5A1
- ALDH7A1
- ALG13
- AMT
- ARFGEF2
- ARG1
- ARHGEF15
- ARHGEF9
- ARX
- ASAH1
- ATP13A2
- ATP7A
- BCKDHB
- BRAT1
- BTD
- CACNA1A
- CACNA2D2
- CACNB4
- CASK
- CDKL5
- CERS1
- CHD2
- CHRNA2
- CHRNA4
- CHRNA7
- CHRNB2
- CLCN2
- CLCN4
- CLN3
- CLN5
- CLN6
- CLN8
- CNTN2
- CNTNAP2
- CSNK1G1
- CSTB
- CTSD
- CTSF
- CYP2C19
- CYP2C9
- CYP2D6
- D2HGDH
- DEPDC5
- DNAJC5
- DNM1
- DOCK7
- DYNC1H1
- EEF1A2
- EPHX1
- EPM2A
- EPM2AIP1
- ERMARD
- FARS2
- FLNA
- FOLR1
- FOXG1
- FUCA1
- GABBR1
- GABBR2
- GABRA1
- GABRA5
- GABRA6
- GABRB1
- GABRB2
- GABRB3
- GABRD
- GABRE
- GABRG1
- GABRG2
- GABRG3
- GABRP
- GABRQ
- GABRR1
- GABRR2
- GABRR3
- GAD2
- GAMT
- GATM
- GCSH
- GLB1
- GLDC
- GLRA1
- GLRB
- GLUL
- GNAO1
- GOSR2
- GPHN
- GRIN1
- GRIN2A
- GRIN2B
- GRN
- HCN1
- HCN2
- HCN3
- HCN4
- HNRNPU
- KCNA2
- KCNAB1
- KCNB1
- KCNC1
- KCNH2
- KCNH5
- KCNJ1
- KCNJ10
- KCNMA1
- KCNQ2
- KCNQ3
- KCNT1
- KCNT2
- KCTD7
- KIF2A
- KIF5C
- KPNA7
- LGI1
- MAGI2
- MAPK10
- MBD5
- MECP2
- MED17
- MEF2C
- MFSD8
- MOCS1
- MOCS2
- MTOR
- MYO5A
- NECAP1
- NEDD4L
- NEU1
- NHLRC1
- NRXN1
- PCDH19
- PGK1
- PIGA
- PIGN
- PIGQ
- PIGT
- PLCB1
- PMM2
- PNKP
- PNPO
- POLG
- PPT1
- PRICKLE1
- PRICKLE2
- PRRT2
- PSAT1
- PURA
- RAB27A
- RAB3GAP1
- RAB3GAP2
- RBFOX1
- RBFOX3
- RFT1
- ROGDI
- SCARB2
- SCN1A
- SCN1B
- SCN2A
- SCN4A
- SCN5A
- SCN8A
- SCN9A
- SERPINI1
- SLC12A1
- SLC12A2
- SLC12A7
- SLC13A5
- SLC25A22
- SLC2A1
- SLC35A2
- SLC4A10
- SLC6A5
- SLC6A8
- SNIP1
- SPTAN1
- SRGAP2
- SRPX2
- ST3GAL3
- ST3GAL5
- STAMBP
- STXBP1
- SUOX
- SYN1
- SYNGAP1
- SZT2
- TBC1D24
- TCF4
- TNK2
- TPP1
- TREX1
- TUBB
- TUBB2A
- TUBB3
- TUBG1
- UBE3A
- VDAC1
- WWOX
EXOMAS
Heterotaxia
Ref. 4006
7 genes
- ACVR2B
- CFAP53
- CFC1
- MMP21
- NODAL
- PKD1L1
- ZIC3
EXOMAS
Síndrome hemolítico urémico atípico
Ref. 4539
10 genes
- C3
- CD46
- CFB
- CFH
- CFHR1
- CFHR3
- CFHR4
- CFI
- DGKE
- THBD
EXOMAS
Ehlers-Danlos, síndrome
Ref. 4065
22 genes
- ADAMTS2
- AEBP1
- ATP7A
- B3GALT6
- B4GALT7
- C1R
- C1S
- CHST14
- COL12A1
- COL1A1
- COL1A2
- COL3A1
- COL5A1
- COL5A2
- DSE
- FKBP14
- FLNA
- PLOD1
- PRDM5
- SLC39A13
- TNXB
- ZNF469
EXOMAS
Epilepsia mioclónica juvenil
Ref. 4265
7 genes
- CACNB4
- CLCN2
- EFHC1
- GABRA1
- GABRD
- ICK
- TBC1D24
EXOMAS
Eritrocitosis familiar
Ref. 3930
7 genes
- EGLN1
- EPAS1
- EPO
- EPOR
- JAK2
- SH2B3
- VHL
EXOMAS
Charcot-Marie-Tooth, síndrome
Ref. 4553
34 genes
- AARS
- ARHGEF10
- DNM2
- DYNC1H1
- EGR2
- FGD4
- FIG4
- GARS
- GDAP1
- GDAP1L1
- GJB1
- HK1
- HSPB1
- HSPB8
- KARS
- KIF1B
- LITAF
- LMNA
- LRSAM1
- MED25
- MFN2
- MPZ
- MTMR2
- NDRG1
- NEFL
- PMP22
- PRPS1
- PRX
- RAB7A
- SBF2
- SH3TC2
- SPTLC1
- TRPV4
- YARS
EXOMAS
Charcot-Marie-Tooth, síndrome
Ref. 4092
34 genes
- AARS
- ARHGEF10
- DNM2
- DYNC1H1
- EGR2
- FGD4
- FIG4
- GARS
- GDAP1
- GDAP1L1
- GJB1
- HK1
- HSPB1
- HSPB8
- KARS
- KIF1B
- LITAF
- LMNA
- LRSAM1
- MED25
- MFN2
- MPZ
- MTMR2
- NDRG1
- NEFL
- PMP22
- PRPS1
- PRX
- RAB7A
- SBF2
- SH3TC2
- SPTLC1
- TRPV4
- YARS
EXOMAS
Charcot-Marie-Tooth, síndrome
Ref. 4269
79 genes
- AARS
- ABHD12
- AIFM1
- ARHGEF10
- ATP1A1
- ATP7A
- BAG3
- BSCL2
- CNTNAP1
- COA7
- COX6A1
- DCAF8
- DCTN2
- DGAT2
- DHTKD1
- DNAJB2
- DNM2
- DNMT1
- DRP2
- DYNC1H1
- EGR2
- FBXO38
- FGD4
- FIG4
- GARS
- GDAP1
- GJB1
- GJB3
- GNB4
- HARS
- HINT1
- HK1
- HSPB1
- HSPB8
- IGHMBP2
- INF2
- JPH1
- KARS
- KIF1B
- KIF5A
- LITAF
- LMNA
- LRSAM1
- MARS
- MCM3AP
- MED25
- MFN2
- MME
- MORC2
- MPV17
- MPZ
- MTMR2
- NAGLU
- NDRG1
- NEFH
- NEFL
- PDK3
- PLEKHG5
- PMP2
- PMP22
- PRPS1
- PRX
- RAB7A
- SBF1
- SBF2
- SCO2
- SGPL1
- SH3TC2
- SIGMAR1
- SPG11
- SPTLC1
- SURF1
- SYT2
- TFG
- TRIM2
- TRPV4
- VCP
- WARS
- YARS
EXOMAS
Charcot-Marie-Tooth, síndrome
Ref. 3568
60 genes
- AARS
- AIFM1
- COX6A1
- DCAF8
- DCTN2
- DGAT2
- DHTKD1
- DNAJB2
- DNM2
- DNMT1
- DYNC1H1
- EGR2
- FBXO38
- FGD4
- FIG4
- GARS
- GDAP1
- GJB1
- GJB3
- GNB4
- HARS
- HK1
- HSPB1
- HSPB8
- IGHMBP2
- INF2
- JPH1
- KARS
- KIF1B
- LITAF
- LMNA
- LRSAM1
- MARS
- MED25
- MFN2
- MME
- MORC2
- MPZ
- MTMR2
- NAGLU
- NDRG1
- NEFH
- NEFL
- PDK3
- PLEKHG5
- PMP22
- PRPS1
- PRX
- RAB7A
- SBF1
- SBF2
- SH3TC2
- SPG11
- SURF1
- SYT2
- TFG
- TRIM2
- TRPV4
- VCP
- YARS
EXOMAS
Dent, enfermedad
Ref. 4756
2 genes
- CLCN5
- OCRL
EXOMAS
Displasia geleofísica
Ref. 3873
3 genes
- ADAMTSL2
- FBN1
- LTBP2
EXOMAS
Déficit de hormonas pituitarias combinado congénito
Ref. 3994
6 genes
- HESX1
- LHX3
- LHX4
- OTX2
- POU1F1
- PROP1
EXOMAS
Cáncer renal papilar de células claras hereditario
Ref. 3901
1 genes
- MET
EXOMAS
Alstrom, síndrome
Ref. 4767
1 genes
- ALMS1
EXOMAS
Adrenocortical nodular pigmentada primaria, enfermedad
Ref. 3984
4 genes
- PDE11A
- PDE8B
- PRKACA
- PRKAR1A
EXOMAS
Meier-Gorlin, síndrome
Ref. 3681
8 genes
- CDC45
- CDC6
- CDT1
- GMNN
- MCM5
- ORC1
- ORC4
- ORC6
EXOMAS
Angiopatía amieloide hereditaria cerebral
Ref. 3986
3 genes
- APP
- CST3
- ITM2B
EXOMAS
QT corto, síndrome
Ref. 3637
5 genes
- CACNA1C
- CACNB2
- KCNH2
- KCNJ2
- KCNQ1
EXOMAS
Bartter, síndrome
Ref. 4088
27 genes
- ATP6V1B1
- BSND
- CA2
- CASR
- CLCNKA
- CLCNKB
- CLDN16
- CLDN19
- FXYD2
- HSD11B2
- KCNJ1
- KCNJ10
- KLHL3
- NR3C2
- SCNN1A
- SCNN1B
- SCNN1G
- SLC12A1
- SLC12A2
- SLC12A3
- SLC12A5
- SLC12A7
- SLC4A1
- SLC4A4
- SLC4A5
- WNK1
- WNK4
EXOMAS
Bartter, síndrome
Ref. 3816
7 genes
- BSND
- CLCNKA
- CLCNKB
- KCNJ1
- MAGED2
- SLC12A1
- SLC12A3
EXOMAS
Diabetes MODY
Ref. 4305
14 genes
- ABCC8
- APPL1
- BLK
- CEL
- GCK
- HNF1A
- HNF1B
- HNF4A
- INS
- KCNJ11
- KLF11
- NEUROD1
- PAX4
- PDX1
EXOMAS
Diabetes MODY
Ref. 4077
11 genes
- BLK
- GCK
- HNF1A
- HNF1B
- HNF4A
- KCNJ11
- KLF11
- NEUROD1
- PAX4
- PDX1
- SLC2A2
EXOMAS
Joubert, síndrome
Ref. 10038
39 genes
- AHI1
- ARL13B
- ARL3
- ARMC9
- B9D1
- B9D2
- C2CD3
- CC2D2A
- CEP104
- CEP120
- CEP290
- CEP41
- CPLANE1
- CSPP1
- FAM149B1
- IFT172
- INPP5E
- KIAA0556
- KIAA0586
- KIF7
- MKS1
- NPHP1
- OFD1
- PDE6D
- PIBF1
- POC1B
- RPGRIP1L
- SUFU
- TCTN1
- TCTN2
- TCTN3
- TMEM107
- TMEM138
- TMEM216
- TMEM231
- TMEM237
- TMEM67
- TTC21B
- ZNF423
EXOMAS
Fiebres familiares recurrentes
Ref. 3781
11 genes
- ELANE
- HTR1A
- LPIN2
- MEFV
- MVK
- NLRC4
- NLRP12
- NLRP3
- PSTPIP1
- TNFAIP3
- TNFRSF1A
EXOMAS
3MC, síndrome
Ref. 3981
3 genes
- COLEC10
- COLEC11
- MASP1
EXOMAS
Miopatías Congénitas
Ref. 4604
32 genes
- ACTA1
- BIN1
- CACNA1S
- CCDC7
- CCDC78
- CFL2
- CNTN1
- DNM2
- HACD1
- KBTBD13
- KLHL40
- KLHL41
- LMOD3
- MAP3K20
- MEGF10
- MTM1
- MTMR14
- MYF6
- MYH7
- MYMK
- MYO18B
- MYPN
- NEB
- RYR1
- SCN4A
- SELENON
- SPEG
- STAC3
- TNNT1
- TPM2
- TPM3
- TTN
EXOMAS
Miopatías Congénitas
Ref. 4081
11 genes
- ACTA1
- CAV3
- DYSF
- FLNC
- GNE
- MATR3
- MTM1
- MYH7
- RYR1
- SELENON
- TPM3
EXOMAS
Hipoacusia no sindrómica
Ref. 4209
112 genes
- ACTG1
- ADCY1
- AIFM1
- ATP2B2
- BDP1
- BSND
- CABP2
- CCDC50
- CD164
- CDC14A
- CDH23
- CEACAM16
- CIB2
- CLDN14
- CLIC5
- COCH
- COL11A2
- COL4A6
- CRYM
- DCDC2
- DIABLO
- DIAPH1
- DMXL2
- DSPP
- ELMOD3
- EPS8
- EPS8L2
- ESPN
- ESRP1
- ESRRB
- EYA4
- FAM189A2
- FOXI1
- GAB1
- GIPC3
- GJB2
- GJB3
- GJB6
- GPRASP2
- GPSM2
- GRHL2
- GRXCR1
- GRXCR2
- GSDME
- HGF
- HOMER2
- ILDR1
- KARS
- KCNJ10
- KCNQ4
- KITLG
- LHFPL5
- LOXHD1
- LRTOMT
- MARVELD2
- MCM2
- MET
- MPZL2
- MSRB3
- MYH14
- MYH9
- MYO15A
- MYO1A
- MYO3A
- MYO6
- MYO7A
- NARS2
- NLRP3
- OSBPL2
- OTOA
- OTOF
- OTOG
- OTOGL
- P2RX2
- PCDH15
- PDE1C
- PDZD7
- PJVK
- PNPT1
- POU3F4
- POU4F3
- PPIP5K2
- PRPS1
- RDX
- RIPOR2
- ROR1
- S1PR2
- SERPINB6
- SIX1
- SLC17A8
- SLC22A4
- SLC26A4
- SLC26A5
- SLC44A4
- SMPX
- STRC
- SYNE4
- TBC1D24
- TECTA
- TJP2
- TMC1
- TMEM132E
- TMIE
- TMPRSS3
- TNC
- TPRN
- TRIOBP
- TSPEAR
- USH1C
- WBP2
- WFS1
- WHRN
EXOMAS
Displasia ectodérmica
Ref. 4568
12 genes
- CST6
- EDA
- EDAR
- EDARADD
- GJB6
- HOXC13
- KDF1
- KREMEN1
- KRT74
- KRT85
- MSX1
- TSPEAR
EXOMAS
Displasia ectodérmica
Ref. 3998
11 genes
- EDA
- EDAR
- EDARADD
- GJB6
- HOXC13
- KDF1
- KREMEN1
- KRT74
- KRT85
- MSX1
- TSPEAR
EXOMAS
Colestasis intrahepática familiar progresiva
Ref. 3738
5 genes
- ABCB11
- ABCB4
- ATP8B1
- NR1H4
- TJP2
EXOMAS
Noonan-like, síndrome
Ref. 4682
22 genes
- A2ML1
- BRAF
- CBL
- HRAS
- KRAS
- LZTR1
- MAP2K1
- MAP2K2
- MRAS
- NF1
- NRAS
- PPP1CB
- PTPN11
- RAF1
- RASA2
- RIT1
- RRAS
- RRAS2
- SHOC2
- SOS1
- SOS2
- SPRED1
EXOMAS
Noonan-like, síndrome
Ref. 4050
20 genes
- A2ML1
- BRAF
- CBL
- HRAS
- KRAS
- LZTR1
- MAP2K1
- MAP2K2
- NF1
- NRAS
- PPP1CB
- PTPN11
- RAF1
- RASA1
- RIT1
- RRAS
- SHOC2
- SOS1
- SOS2
- SPRED1
EXOMAS
Angelman-like, síndrome
Ref. 3660
12 genes
- ADSL
- CDKL5
- EHMT1
- HERC2
- MBD5
- MECP2
- MTHFR
- SLC9A6
- TCF4
- UBE3A
- WAC
- ZEB2
EXOMAS
Craneosinostosis
Ref. 4715
21 genes
- ALPL
- ALX4
- CDC45
- CYP26B1
- ERF
- FGFR1
- FGFR2
- FGFR3
- IL11RA
- MEGF8
- MSX2
- POR
- RAB23
- RECQL4
- SKI
- SMAD6
- SMO
- TCF12
- TWIST1
- WDR35
- ZIC1
EXOMAS
Craneosinostosis
Ref. 3882
20 genes
- ALPL
- ALX4
- CDC45
- CYP26B1
- ERF
- FGFR1
- FGFR2
- FGFR3
- IL11RA
- MEGF8
- MSX2
- RAB23
- RECQL4
- SKI
- SMAD6
- SMO
- TCF12
- TWIST1
- WDR35
- ZIC1
EXOMAS
Usher, síndrome
Ref. 4330
13 genes
- ADGRV1
- ARSG
- CDH23
- CIB2
- CLRN1
- HARS
- MYO7A
- PCDH15
- PDZD7
- USH1C
- USH1G
- USH2A
- WHRN
EXOMAS
Paraplejias espásticas
Ref. 4511
62 genes
- ALS2
- AMPD2
- AP4B1
- AP4E1
- AP4M1
- AP4S1
- AP5Z1
- ARL6IP1
- ARSI
- ATL1
- B4GALNT1
- BICD2
- BSCL2
- C12orf65
- C19orf12
- CCT5
- CYP2U1
- CYP7B1
- DDHD1
- DDHD2
- ENTPD1
- ERLIN1
- ERLIN2
- FA2H
- FLRT1
- GAD1
- GBA2
- GJC2
- GRID2
- HSPD1
- KIF1A
- KIF1C
- KIF5A
- L1CAM
- LYST
- MAG
- MARS
- NIPA1
- NT5C2
- PGAP1
- PLP1
- PNPLA6
- RAB3GAP2
- REEP1
- REEP2
- RTN2
- SLC16A2
- SLC33A1
- SPART
- SPAST
- SPG11
- SPG21
- SPG7
- TECPR2
- TFG
- USP8
- VPS37A
- WASHC5
- WDR48
- ZFR
- ZFYVE26
- ZFYVE27
EXOMAS
Paraplejias espásticas
Ref. 4085
32 genes
- AP4B1
- AP4E1
- AP4M1
- AP4S1
- AP5Z1
- ATL1
- BSCL2
- C12orf65
- C19orf12
- CYP7B1
- ENTPD1
- ERLIN2
- FA2H
- GJC2
- HSPD1
- KIF1A
- KIF5A
- L1CAM
- NIPA1
- PLP1
- PNPLA6
- REEP1
- RTN2
- SLC33A1
- SPART
- SPAST
- SPG11
- SPG21
- SPG7
- WASHC5
- ZFYVE26
- ZFYVE27
EXOMAS
Paraplejias espásticas
Ref. 4302
72 genes
- ADAR
- ALDH18A1
- ALDH3A2
- AMPD2
- AP4B1
- AP4E1
- AP4M1
- AP4S1
- AP5Z1
- ARL6IP1
- ATAD3A
- ATL1
- ATP13A2
- ATP2B4
- B4GALNT1
- BICD2
- BSCL2
- C12orf65
- C19orf12
- CAPN1
- CPT1C
- CYP2U1
- CYP7B1
- DDHD1
- DDHD2
- DNM2
- DSTYK
- ENTPD1
- ERLIN1
- ERLIN2
- FA2H
- FARS2
- GAD1
- GBA2
- GJC2
- GRID2
- HSPD1
- IBA57
- KIF1A
- KIF1C
- KIF5A
- KLC2
- KLC4
- L1CAM
- MAG
- MARS
- NIPA1
- NT5C2
- PGAP1
- PLP1
- PNPLA6
- REEP1
- REEP2
- RTN2
- SLC16A2
- SLC33A1
- SPART
- SPAST
- SPG11
- SPG21
- SPG7
- TECPR2
- TFG
- TUBB4A
- UBAP1
- UCHL1
- USP8
- VPS37A
- WASHC5
- WDR48
- ZFYVE26
- ZFYVE27
EXOMAS
Linfohistiocitosis hemofagocítica familiar
Ref. 3855
7 genes
- PRF1
- RAB27A
- SH2D1A
- STX11
- STXBP2
- UNC13D
- XIAP
EXOMAS
Sindrome de Waardenburg
Ref. 3734
7 genes
- EDN3
- EDNRB
- MITF
- PAX3
- SNAI2
- SOX10
- TYR
EXOMAS
Calcinosis bilateral estriato-pálido-dentada
Ref. 3987
4 genes
- PDGFB
- PDGFRB
- SLC20A2
- XPR1
EXOMAS
Microcefalia
Ref. 4200
88 genes
- AMPD2
- ANKLE2
- ARFGEF2
- ASPM
- ATR
- ATRIP
- ATRX
- C7orf43
- CASK
- CDC45
- CDC6
- CDK5RAP2
- CDK6
- CDKL5
- CDT1
- CENPE
- CENPJ
- CEP135
- CEP152
- CEP63
- CHMP1A
- CIT
- CLP1
- COASY
- COPB2
- CTNNA2
- DHCR7
- EXOSC3
- EXOSC8
- EXOSC9
- FOXG1
- GMNN
- IER3IP1
- KIF14
- KIF2A
- KIF5C
- KNL1
- MCM5
- MCPH1
- MECP2
- MED17
- MFSD2A
- MYCN
- NCAPD2
- NCAPD3
- NCAPH
- NDE1
- NIN
- NUP37
- ORC1
- ORC4
- ORC6
- PCLO
- PCNT
- PHC1
- PNKP
- RAB18
- RAB3GAP1
- RAB3GAP2
- RARS2
- RBBP8
- SASS6
- SEPSECS
- SLC25A19
- SLC2A1
- SLC9A6
- STIL
- TBC1D20
- TBC1D23
- TCF4
- TOE1
- TSEN15
- TSEN2
- TSEN34
- TSEN54
- TUBA8
- TUBB
- TUBB2A
- TUBB2B
- TUBB3
- TUBG1
- UBE3A
- VPS53
- VRK1
- WDFY3
- WDR62
- ZEB2
- ZNF335
EXOMAS
Parkinson, enfermedad
Ref. 4309
29 genes
- ADH1C
- ATP13A2
- ATXN2
- CHCHD2
- DNAJC13
- DNAJC6
- EIF4G1
- FBXO7
- GBA
- GIGYF2
- GLUD2
- HTRA2
- LRRK2
- MAPT
- PARK7
- PINK1
- PLA2G6
- PODXL
- PRKN
- RIC3
- SLC6A3
- SNCA
- SYNJ1
- TAF1
- TBP
- TMEM230
- UCHL1
- VPS13C
- VPS35
EXOMAS
Parkinson, enfermedad
Ref. 4512
20 genes
- ATP13A2
- ATP1A3
- ATP6AP2
- DNAJC6
- EIF4G1
- FBXO7
- GBA
- GIGYF2
- HTRA2
- LRRK2
- PARK7
- PINK1
- PLA2G6
- POLG
- PRKN
- SNCA
- SNCAIP
- SYNJ1
- UCHL1
- VPS35
EXOMAS
Heterotopia nodular periventricular
Ref. 4540
9 genes
- ARF1
- ARFGEF2
- DCHS1
- ERMARD
- FAT4
- FLNA
- FMR1
- LRP2
- NEDD4L
EXOMAS
Distonía
Ref. 4622
24 genes
- ACTB
- ANO3
- ATP1A3
- CACNA1B
- COL6A3
- DRD2
- GCH1
- GNAL
- HPCA
- KCTD17
- KMT2B
- MECR
- MR1
- PNKD
- PRKRA
- PRRT2
- SGCE
- SLC2A1
- SPR
- TAF1
- TH
- THAP1
- TOR1A
- TUBB4A
EXOMAS
Distonía
Ref. 3664
23 genes
- ACTB
- ANO3
- ATP1A3
- CACNA1B
- COL6A3
- DRD2
- GCH1
- GNAL
- HPCA
- KCTD17
- KMT2B
- MECR
- MR1
- PRKRA
- PRRT2
- SGCE
- SLC2A1
- SPR
- TAF1
- TH
- THAP1
- TOR1A
- TUBB4A
EXOMAS
3M, Síndrome
Ref. 3980
3 genes
- CCDC8
- CUL7
- OBSL1
EXOMAS
Leucodistrofia
Ref. 4557
68 genes
- ABCD1
- ACOX1
- ADAR
- AIMP1
- AIMP2
- ALDH3A2
- ARSA
- ASPA
- CSF1R
- CYP27A1
- DARS2
- DEGS1
- EARS2
- EIF2B1
- EIF2B2
- EIF2B3
- EIF2B4
- EIF2B5
- EPRS
- FAM126A
- FUCA1
- GALC
- GBE1
- GFAP
- GJA1
- GJC2
- HEPACAM
- HIKESHI
- HSD17B4
- HSPD1
- L2HGDH
- LMNB1
- MLC1
- PEX1
- PEX10
- PEX11B
- PEX12
- PEX13
- PEX14
- PEX16
- PEX19
- PEX2
- PEX26
- PEX3
- PEX5
- PEX6
- PEX7
- PLP1
- POLR1C
- POLR3A
- POLR3B
- PSAP
- PYCR2
- RARS
- RNASEH2A
- RNASEH2B
- RNASEH2C
- RNASET2
- SAMHD1
- SCP2
- SLC17A5
- SOX10
- SUMF1
- TMEM106B
- TREX1
- TUBB4A
- UFM1
- VPS11
EXOMAS
Amelogénesis imperfecta
Ref. 3716
16 genes
- ACP4
- AMBN
- AMELX
- AMTN
- DLX3
- ENAM
- FAM20A
- FAM83H
- GPR68
- ITGB6
- KLK4
- LAMB3
- MMP20
- ODAPH
- SLC24A4
- WDR72
EXOMAS
Hermansky-Pudlak, Síndrome
Ref. 3733
10 genes
- AP3B1
- AP3D1
- BLOC1S3
- BLOC1S6
- DTNBP1
- HPS1
- HPS3
- HPS4
- HPS5
- HPS6
EXOMAS
Esquisencefalia
Ref. 3843
4 genes
- COL4A1
- EMX2
- SHH
- SIX3
EXOMAS
Charcot-Marie-Tooth Axonal
Ref. 4261
60 genes
- AARS
- AIFM1
- ATP1A1
- ATP7A
- BAG3
- BSCL2
- CNTNAP1
- COA7
- DCAF8
- DCTN2
- DGAT2
- DHTKD1
- DNAJB2
- DNM2
- DNMT1
- DYNC1H1
- FBXO38
- GARS
- GDAP1
- GJB1
- GJB3
- HARS
- HINT1
- HSPB1
- HSPB8
- IGHMBP2
- INF2
- JPH1
- KIF1B
- KIF5A
- LMNA
- LRSAM1
- MARS
- MCM3AP
- MED25
- MFN2
- MME
- MORC2
- MPV17
- MPZ
- NAGLU
- NEFH
- NEFL
- PDK3
- PRX
- RAB7A
- SBF1
- SCO2
- SGPL1
- SH3TC2
- SIGMAR1
- SPG11
- SPTLC1
- SYT2
- TFG
- TRIM2
- TRPV4
- VCP
- WARS
- YARS
EXOMAS
Cutis laxa
Ref. 3992
9 genes
- ALDH18A1
- ATP6V0A2
- ATP6V1A
- ATP6V1E1
- EFEMP2
- ELN
- FBLN5
- LTBP4
- PYCR1
EXOMAS
Neoplasia endocrina múltiple hereditaria
Ref. 3898
2 genes
- MEN1
- RET
EXOMAS
Epilepsia
Ref. 4091
46 genes
- ADSL
- ARX
- CACNB4
- CDKL5
- CHRNA2
- CHRNA4
- CHRNB2
- CLCN2
- CLN3
- CLN5
- CLN6
- CLN8
- CNTNAP2
- CSTB
- CTSD
- EFHC1
- EPM2A
- FOXG1
- GABRA1
- GABRG2
- GAMT
- GATM
- KCNQ2
- KCNQ3
- LGI1
- MECP2
- MFSD8
- NHLRC1
- NRXN1
- PCDH19
- PLCB1
- PNKP
- POLG
- PPT1
- PRICKLE1
- SCN1A
- SCN1B
- SCN2A
- SLC2A1
- SLC9A6
- STXBP1
- SYN1
- TCF4
- TPP1
- UBE3A
- ZEB2
EXOMAS
Epilepsia
Ref. 3797
171 genes
- AARS
- ABAT
- ADAM22
- ADGRG1
- ADGRV1
- ADSL
- ALDH7A1
- ALG13
- AP3B2
- ARFGEF2
- ARHGEF9
- ARV1
- ARX
- ATP1A2
- CACNA1A
- CACNA1H
- CACNB4
- CAD
- CASR
- CBL
- CDKL5
- CERS1
- CHD2
- CHRNA2
- CHRNA4
- CHRNB2
- CLCN2
- CLN3
- CLN5
- CLN6
- CLN8
- CNPY3
- CNTNAP2
- CPA6
- CSTB
- CTSD
- CTSF
- DCX
- DENND5A
- DEPDC5
- DNAJC5
- DNM1
- DOCK7
- EEF1A2
- EFHC1
- EPM2A
- FGF12
- FOLR1
- FOXG1
- FOXRED1
- FRRS1L
- GABBR2
- GABRA1
- GABRB1
- GABRB3
- GABRD
- GABRG2
- GAMT
- GATM
- GNAO1
- GOSR2
- GRIN2A
- GRIN2B
- GRIN2D
- GRN
- GUF1
- HCN1
- HNRNPU
- IQSEC2
- ITPA
- KCNA2
- KCNB1
- KCNC1
- KCNJ10
- KCNMA1
- KCNQ2
- KCNQ3
- KCNT1
- KCNT2
- KCTD7
- LGI1
- LIAS
- LMNB2
- MDH2
- MECP2
- MEF2C
- MFSD8
- MTHFR
- NDE1
- NDUFA1
- NDUFA11
- NDUFAF1
- NDUFAF2
- NDUFAF3
- NDUFAF4
- NDUFAF5
- NDUFB11
- NDUFB3
- NDUFB9
- NDUFS1
- NDUFS3
- NDUFS4
- NDUFS6
- NDUFV1
- NDUFV2
- NECAP1
- NEDD4L
- NHLRC1
- NPRL2
- NPRL3
- NRXN1
- NTRK2
- NUBPL
- OPHN1
- PAFAH1B1
- PCDH19
- PHF6
- PIGA
- PIGO
- PIGP
- PLCB1
- PNKP
- PNPO
- POLG
- POLG2
- PPT1
- PRDM8
- PRICKLE1
- PRICKLE2
- PRRT2
- RELN
- SCARB2
- SCN1A
- SCN1B
- SCN2A
- SCN3A
- SCN8A
- SCN9A
- SIK1
- SLC12A5
- SLC13A5
- SLC19A3
- SLC1A2
- SLC25A12
- SLC25A22
- SLC2A1
- SLC35A2
- SLC9A6
- SPTAN1
- SRPX2
- ST3GAL3
- ST3GAL5
- STX1B
- STXBP1
- SYN1
- SYNJ1
- SZT2
- TBC1D24
- TCF4
- TIMMDC1
- TMEM126B
- TPP1
- TSC1
- TSC2
- TSEN54
- UBA5
- UBE3A
- WDR62
- WWOX
- YWHAG
- ZEB2
EXOMAS
Epilepsia
Ref. 4267
185 genes
- AARS
- ABAT
- ACTL6B
- ADAM22
- ADGRG1
- ADGRV1
- ADSL
- ALDH7A1
- ALG13
- AP3B2
- ARFGEF2
- ARHGEF9
- ARV1
- ARX
- ATP1A2
- CACNA1A
- CACNA1E
- CACNA1H
- CACNB4
- CAD
- CASR
- CBL
- CDKL5
- CERS1
- CHD2
- CHRNA2
- CHRNA4
- CHRNB2
- CLCN2
- CLN3
- CLN5
- CLN6
- CLN8
- CNPY3
- CNTNAP2
- CPA6
- CPLX1
- CSTB
- CTSD
- CTSF
- CUX2
- CYFIP2
- DCX
- DENND5A
- DEPDC5
- DNAJC5
- DNM1
- DOCK7
- EEF1A2
- EFHC1
- EPM2A
- FGF12
- FOLR1
- FOXG1
- FOXRED1
- FRRS1L
- GABBR2
- GABRA1
- GABRB1
- GABRB3
- GABRD
- GABRG2
- GAMT
- GATM
- GLS
- GNAO1
- GOSR2
- GRIN2A
- GRIN2B
- GRIN2D
- GRN
- GUF1
- HCN1
- HNRNPU
- ICK
- IQSEC2
- ITPA
- KCNA2
- KCNB1
- KCNC1
- KCNJ10
- KCNMA1
- KCNQ2
- KCNQ3
- KCNT1
- KCNT2
- KCTD7
- LGI1
- LIAS
- LMNB2
- MDH2
- MECP2
- MEF2C
- MFSD8
- MTHFR
- NDE1
- NDUFA1
- NDUFA11
- NDUFAF1
- NDUFAF2
- NDUFAF3
- NDUFAF4
- NDUFAF5
- NDUFB11
- NDUFB3
- NDUFB9
- NDUFS1
- NDUFS3
- NDUFS4
- NDUFS6
- NDUFV1
- NDUFV2
- NECAP1
- NEDD4L
- NEUROD2
- NHLRC1
- NPRL2
- NPRL3
- NRXN1
- NTRK2
- NUBPL
- OPHN1
- PACS2
- PAFAH1B1
- PARS2
- PCDH19
- PHACTR1
- PHF6
- PIGA
- PIGO
- PIGP
- PLCB1
- PNKP
- PNPO
- POLG
- POLG2
- PPT1
- PRDM8
- PRICKLE1
- PRICKLE2
- PRRT2
- RELN
- RHOBTB2
- RNF13
- SCARB2
- SCN1A
- SCN1B
- SCN2A
- SCN3A
- SCN8A
- SCN9A
- SIK1
- SLC12A5
- SLC13A5
- SLC19A3
- SLC1A2
- SLC25A12
- SLC25A22
- SLC2A1
- SLC35A2
- SLC9A6
- SPTAN1
- SRPX2
- ST3GAL3
- ST3GAL5
- STX1B
- STXBP1
- SYN1
- SYNJ1
- SZT2
- TBC1D24
- TCF4
- TIMMDC1
- TMEM126B
- TPP1
- TRAK1
- TSC1
- TSC2
- TSEN54
- UBA5
- UBE3A
- WDR62
- WWOX
- YWHAG
- ZEB2
EXOMAS
Defectos del cierre del tubo neural
Ref. 3993
5 genes
- CCL2
- FUZ
- TBXT
- VANGL1
- VANGL2
EXOMAS
Discapacidad Intelectual
Ref. 4044
799 genes
- AAAS
- AASS
- ABAT
- ABCD1
- ABHD5
- ACADS
- ACO2
- ACOX1
- ACSF3
- ACSL4
- ACTB
- ACTG1
- ACY1
- ADAMTSL2
- ADAR
- ADAT3
- ADD3
- ADGRG1
- ADK
- ADNP
- ADRA2B
- ADSL
- AFF2
- AFF4
- AGA
- AGTR2
- AHDC1
- AHI1
- AIMP1
- AKT3
- ALDH18A1
- ALDH3A2
- ALDH4A1
- ALDH5A1
- ALDH7A1
- ALDOA
- ALG1
- ALG11
- ALG12
- ALG13
- ALG2
- ALG3
- ALG6
- ALG9
- ALX3
- ALX4
- AMPD2
- AMT
- ANK3
- ANKRD11
- ANTXR1
- AP1S2
- AP3B1
- AP4B1
- AP4E1
- AP4M1
- AP4S1
- APOPT1
- APTX
- ARFGEF2
- ARG1
- ARHGEF6
- ARHGEF9
- ARID1A
- ARID1B
- ARID2
- ARL13B
- ARL6
- ARNT2
- ARX
- ASCL1
- ASH1L
- ASL
- ASNS
- ASPA
- ASPM
- ASS1
- ASXL1
- ASXL3
- ATIC
- ATP1A2
- ATP2A2
- ATP6AP2
- ATP6V0A2
- ATP7A
- ATP8A2
- ATR
- ATRX
- AUH
- AUTS2
- B3GALNT2
- B3GLCT
- B4GALT1
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- BCKDHA
- BCKDHB
- BCL11A
- BCOR
- BCS1L
- BLM
- BMPER
- BRAF
- BRF1
- BRWD3
- BSCL2
- BSND
- BTD
- BUB1B
- C12orf57
- C12orf65
- C2CD3
- CA2
- CA8
- CACNA1G
- CACNG2
- CAMK2A
- CAMK2B
- CAMTA1
- CASK
- CBL
- CBS
- CC2D1A
- CC2D2A
- CCDC22
- CCDC28B
- CCDC78
- CCDC88C
- CDH15
- CDK5RAP2
- CDK6
- CDKL5
- CDKN1C
- CDON
- CENPJ
- CEP135
- CEP152
- CEP290
- CEP41
- CEP57
- CEP63
- CERS1
- CHAMP1
- CHD2
- CHD7
- CHD8
- CHKB
- CHMP1A
- CIC
- CLCN4
- CLCNKB
- CLIC2
- CLN3
- CLN5
- CLN6
- CLN8
- CLPB
- CLTC
- CNKSR2
- CNNM2
- CNTNAP2
- COG1
- COG6
- COG8
- COL4A1
- COL4A3BP
- COQ2
- COX10
- COX14
- COX15
- COX20
- COX6B1
- COX7B
- CPLANE1
- CPLX1
- CPS1
- CRADD
- CRBN
- CREBBP
- CSPP1
- CTBP1
- CTCF
- CTDP1
- CTNNB1
- CTSA
- CTSD
- CUL4B
- CWF19L1
- CYB5R3
- D2HGDH
- DAG1
- DBT
- DCAF17
- DCHS1
- DCX
- DDHD2
- DDX11
- DDX3X
- DDX59
- DEAF1
- DHCR7
- DKC1
- DLAT
- DLG3
- DMD
- DMPK
- DNAJC19
- DNM1
- DNMT3B
- DOCK8
- DPAGT1
- DPM1
- DPP6
- DPYD
- DPYS
- DYM
- DYNC1H1
- DYRK1A
- EBP
- EDC3
- EEF1A2
- EFTUD2
- EHMT1
- EIF2AK3
- EIF2S3
- EIF4A3
- ELOVL4
- ELP2
- EPB41L1
- ERCC2
- ERCC3
- ERCC6
- ERCC8
- ERLIN2
- ESCO2
- ETHE1
- EXOSC3
- EZH2
- FAM126A
- FANCA
- FANCC
- FANCD2
- FANCE
- FAR1
- FASTKD2
- FAT4
- FBN1
- FBXL4
- FBXO31
- FGD1
- FGFR1
- FGFR2
- FGFR3
- FH
- FKRP
- FKTN
- FLNA
- FMN2
- FMR1
- FOLR1
- FOXG1
- FOXP1
- FOXP2
- FOXRED1
- FRAS1
- FRMPD4
- FTSJ1
- FUCA1
- GABRA1
- GAD1
- GALC
- GALE
- GALT
- GAMT
- GATAD2B
- GATM
- GCH1
- GCK
- GCSH
- GDI1
- GFAP
- GJC2
- GK
- GLB1
- GLDC
- GLI3
- GLYCTK
- GMPPA
- GMPPB
- GNAO1
- GNAS
- GNB1
- GNPAT
- GNPTAB
- GNS
- GORAB
- GPC3
- GPHN
- GPT2
- GRIA3
- GRID2
- GRIK2
- GRIN1
- GRIN2A
- GRIN2B
- GSS
- GTF2H5
- GUSB
- HCCS
- HCFC1
- HCN1
- HDAC4
- HDAC8
- HEPACAM
- HERC2
- HEXA
- HIVEP2
- HLCS
- HMGB3
- HNMT
- HPD
- HPRT1
- HRAS
- HSD17B10
- HSPD1
- HUWE1
- IDS
- IDUA
- IER3IP1
- IGBP1
- IGF1
- IKBKG
- IL1RAPL1
- IMPA1
- INPP5E
- IQSEC2
- ISPD
- ITGA7
- ITPR1
- JAG1
- KANK1
- KANSL1
- KAT6A
- KAT6B
- KATNB1
- KCNA2
- KCNH1
- KCNJ1
- KCNJ10
- KCNJ11
- KCNK9
- KCNQ2
- KCNQ5
- KCTD7
- KDM5C
- KDM6A
- KDM6B
- KIF11
- KIF1A
- KIF1BP
- KIF2A
- KIF4A
- KIF5C
- KIF7
- KIRREL3
- KLHL15
- KMT2C
- KMT2D
- KMT5B
- KNL1
- KPTN
- KRAS
- L1CAM
- L2HGDH
- LAMA1
- LAMA2
- LAMP2
- LARGE1
- LARP7
- LARS
- LAS1L
- LIAS
- LIG4
- LINS1
- LMAN2L
- LONP1
- LRP2
- LRPPRC
- LYRM7
- MAF
- MAGEL2
- MAN1B1
- MAN2B1
- MANBA
- MAOA
- MAP2K1
- MAP2K2
- MAT1A
- MBD5
- MBOAT7
- MBTPS2
- MCCC1
- MCCC2
- MCOLN1
- MCPH1
- MECP2
- MED12
- MED13L
- MED17
- MED23
- MEF2C
- METTL23
- MFSD8
- MGAT2
- MID1
- MID2
- MIR17HG
- MKKS
- MKS1
- MLYCD
- MMACHC
- MMADHC
- MOCS1
- MOCS2
- MOGS
- MPDU1
- MPDZ
- MPV17
- MRPS22
- MTFMT
- MTHFR
- MTO1
- MTOR
- MTR
- MTRR
- MYCN
- MYO5A
- MYT1L
- NAA10
- NAA15
- NAGA
- NAGLU
- NBN
- NDE1
- NDP
- NDST1
- NDUFA1
- NDUFA11
- NDUFA12
- NDUFS1
- NDUFS2
- NDUFS3
- NDUFS4
- NDUFS7
- NDUFS8
- NDUFV1
- NEDD4L
- NEU1
- NEXMIF
- NF1
- NFIA
- NFIX
- NHS
- NIPBL
- NKX2-1
- NLGN3
- NLGN4X
- NONO
- NOP10
- NPC1
- NPC2
- NPHP1
- NR2F1
- NRAS
- NRXN1
- NSD1
- NSDHL
- NSUN2
- NTRK1
- NUP62
- NUS1
- OCLN
- OCRL
- OFD1
- OGT
- OPHN1
- ORC1
- OTC
- PACS1
- PAFAH1B1
- PAH
- PAK3
- PANK2
- PAX1
- PC
- PCDH19
- PCNT
- PDE4D
- PDHA1
- PDHX
- PDP1
- PDSS1
- PEPD
- PET100
- PEX1
- PEX10
- PEX11B
- PEX12
- PEX13
- PEX16
- PEX19
- PEX2
- PEX3
- PEX5
- PEX6
- PEX7
- PGAP1
- PGAP2
- PGK1
- PGM3
- PHF6
- PHF8
- PHGDH
- PHIP
- PIGA
- PIGC
- PIGG
- PIGL
- PIGN
- PIGO
- PIGT
- PIGV
- PIGW
- PIK3R2
- PLA2G6
- PLCB1
- PLK4
- PLP1
- PMM2
- PNKP
- PNP
- PNPLA6
- POGZ
- POLG
- POLR3A
- POLR3B
- POMGNT1
- POMK
- POMT1
- POMT2
- PORCN
- POU1F1
- PPP2R1A
- PPP2R5D
- PPT1
- PQBP1
- PRMT7
- PRODH
- PRPS1
- PRSS12
- PSAP
- PSPH
- PTCH1
- PTCHD1
- PTEN
- PTPN11
- PTRH2
- PTS
- PUF60
- PURA
- PUS1
- PUS3
- PYCR1
- QDPR
- RAB18
- RAB39B
- RAB3GAP1
- RAB3GAP2
- RAC1
- RAD21
- RAF1
- RAI1
- RANBP2
- RARS2
- RBBP8
- RBM10
- RBM28
- RBMX
- RECQL4
- RELN
- RFT1
- RIT1
- RLIM
- RNASEH2A
- RNASEH2B
- RNASEH2C
- RNASET2
- RNF125
- ROGDI
- ROR2
- RPGRIP1L
- RPS6KA3
- RRM2B
- RTTN
- RUBCN
- RUSC2
- SALL1
- SASS6
- SATB2
- SC5D
- SCAPER
- SCN1A
- SCN2A
- SCN8A
- SCO1
- SCO2
- SDCCAG8
- SDHA
- SDHAF1
- SEMA3E
- SEPSECS
- SERAC1
- SETBP1
- SETD2
- SETD5
- SGSH
- SHANK2
- SHANK3
- SHH
- SHOC2
- SHROOM4
- SIL1
- SIX3
- SKI
- SLC12A6
- SLC16A2
- SLC17A5
- SLC1A1
- SLC25A15
- SLC2A1
- SLC35A1
- SLC35A3
- SLC35C1
- SLC4A4
- SLC6A1
- SLC6A17
- SLC6A19
- SLC6A3
- SLC6A8
- SLC7A7
- SLC9A6
- SMAD4
- SMARCA2
- SMARCA4
- SMARCB1
- SMARCE1
- SMC1A
- SMC3
- SMOC1
- SMPD1
- SMS
- SNAP29
- SNIP1
- SNRPN
- SOBP
- SOS1
- SOX10
- SOX11
- SOX2
- SOX3
- SOX5
- SPECC1L
- SPG11
- SPTAN1
- SRCAP
- SRD5A3
- SRPX2
- SSR4
- ST3GAL3
- ST3GAL5
- STAG1
- STIL
- STRA6
- STT3A
- STT3B
- STXBP1
- SUCLA2
- SUCLG1
- SUMF1
- SUOX
- SURF1
- SYN1
- SYNGAP1
- SYP
- TACO1
- TAF1
- TAF13
- TAF2
- TAF6
- TAT
- TBC1D20
- TBC1D24
- TBC1D7
- TBCE
- TBL1XR1
- TCF4
- TCN2
- TCTN2
- TCTN3
- TECR
- TFAP2A
- TGFBR2
- THOC2
- THOC6
- TIMM8A
- TMCO1
- TMEM165
- TMEM216
- TMEM231
- TMEM237
- TMEM240
- TMEM67
- TMLHE
- TNIK
- TRAPPC9
- TREX1
- TRIM32
- TRIO
- TRIP12
- TRMT10A
- TSC1
- TSC2
- TSEN54
- TSFM
- TSHB
- TSPAN7
- TTC19
- TTC8
- TTI2
- TUBA1A
- TUBA8
- TUBB2B
- TUBB3
- TUBGCP6
- TUSC3
- TWIST1
- TWNK
- UBE2A
- UBE3A
- UBE3B
- UBR1
- UPB1
- UPF3B
- UQCRQ
- UROC1
- USP27X
- USP9X
- VLDLR
- VPS13B
- VPS37A
- VPS53
- VRK1
- WAC
- WASHC4
- WDR19
- WDR45
- WDR45B
- WDR62
- WDR73
- WDR81
- WNT5A
- WWOX
- XPA
- XPNPEP3
- XPR1
- XYLT1
- YY1
- ZBTB16
- ZBTB18
- ZBTB24
- ZC3H14
- ZC4H2
- ZDHHC15
- ZDHHC9
- ZEB2
- ZFYVE26
- ZIC2
- ZMYND11
- ZNF526
- ZNF592
- ZNF711
- ZSWIM6
EXOMAS
Autismo
Ref. 4317
196 genes
- ACHE
- ADCY3
- ADCY5
- ADNP
- ADSL
- AKAP9
- ALDH5A1
- AMT
- ANK2
- ANK3
- ANKRD11
- AP1S2
- APH1A
- ARID1B
- ARX
- ASH1L
- ASPM
- ASXL3
- ATP10A
- ATRX
- AUTS2
- AVPR1A
- BAZ2B
- BCKDK
- BCL11A
- CACNA1A
- CACNA1C
- CACNA1D
- CACNA1H
- CACNA2D3
- CASK
- CDKL5
- CEP41
- CHD2
- CHD7
- CHD8
- CIC
- CLN3
- CLN5
- CLN6
- CLN8
- CNKSR2
- CNOT3
- CNTN4
- CNTNAP2
- CREBBP
- CTCF
- CTNNB1
- CTNND2
- CUL3
- CUX1
- DDX3X
- DEAF1
- DHCR7
- DIP2C
- DLGAP2
- DMD
- DNAJC5
- DPYD
- DSCAM
- DYNC1H1
- DYRK1A
- EHMT1
- EIF4E
- ERBIN
- FMR1
- FOXG1
- FOXP1
- GABRB3
- GATM
- GIGYF2
- GRIA1
- GRIA3
- GRIN1
- GRIN2A
- GRIN2B
- GRIP1
- GRN
- HCN1
- HDAC8
- HERC2
- HNRNPU
- HOXA1
- IL1RAPL1
- ILF2
- INTS6
- IQSEC2
- IRF2BPL
- JMJD1C
- KAT2B
- KATNAL2
- KCND2
- KCNJ10
- KDM5B
- KDM5C
- KDM6A
- KMT2A
- KMT2C
- KMT5B
- LEO1
- MACROD2
- MAGEL2
- MAOA
- MBD5
- MBOAT7
- MECP2
- MED12
- MED13
- MED13L
- MEF2C
- MET
- MYT1L
- NAA15
- NCKAP1
- NCOR1
- NEXMIF
- NHS
- NIPBL
- NLGN3
- NLGN4X
- NRXN1
- NRXN3
- NSD1
- NTNG1
- OPHN1
- PAFAH1B1
- PAH
- PCDH19
- PDE4D
- PHF3
- PHIP
- POGZ
- PPM1D
- PPT1
- PQBP1
- PTCHD1
- PTEN
- PTPN11
- RAB39B
- RAI1
- RANBP17
- RELN
- RERE
- RIMS1
- RPL10
- SATB2
- SCN2A
- SCN8A
- SCN9A
- SEMA3E
- SEMA5A
- SET
- SETBP1
- SETD2
- SETD5
- SHANK2
- SHANK3
- SIN3A
- SLC6A1
- SLC6A8
- SLC9A6
- SLC9A9
- SMAD4
- SMARCC2
- SMC1A
- SMC3
- SOX5
- SPAST
- SRCAP
- SRSF11
- SYN1
- SYNGAP1
- TAOK2
- TBL1XR1
- TBR1
- TCF20
- TCF4
- TMLHE
- TNRC6B
- TRAPPC9
- TRIO
- TRIP12
- TSC1
- TSC2
- UBE3A
- UBN2
- UPF3B
- USP15
- USP7
- VPS13B
- WAC
- WDFY3
- WDR62
- ZBTB20
- ZEB2
- ZMYND11
EXOMAS
Autismo
Ref. 3838
189 genes
- ACHE
- ADCY3
- ADCY5
- ADNP
- ADSL
- AKAP9
- ALDH5A1
- AMT
- ANK2
- ANK3
- ANKRD11
- AP1S2
- APH1A
- ARID1B
- ARX
- ASH1L
- ASPM
- ASXL3
- ATP10A
- ATRX
- AUTS2
- AVPR1A
- BAZ2B
- BCKDK
- BCL11A
- CACNA1A
- CACNA1C
- CACNA1D
- CACNA1H
- CACNA2D3
- CASK
- CDKL5
- CHD2
- CHD7
- CHD8
- CIC
- CLN3
- CLN5
- CLN6
- CLN8
- CNKSR2
- CNTN4
- CNTNAP2
- CREBBP
- CTCF
- CTNNB1
- CTNND2
- CUL3
- DDX3X
- DEAF1
- DHCR7
- DIP2C
- DLGAP2
- DMD
- DNAJC5
- DPYD
- DSCAM
- DYNC1H1
- DYRK1A
- EHMT1
- EIF4E
- ERBIN
- FMR1
- FOXG1
- FOXP1
- GABRB3
- GATM
- GIGYF2
- GRIA1
- GRIA3
- GRIN1
- GRIN2A
- GRIN2B
- GRIP1
- GRN
- HCN1
- HDAC8
- HERC2
- HNRNPU
- HOXA1
- IL1RAPL1
- ILF2
- INTS6
- IQSEC2
- IRF2BPL
- JMJD1C
- KAT2B
- KATNAL2
- KCND2
- KCNJ10
- KDM5B
- KDM5C
- KDM6A
- KMT2A
- KMT2C
- KMT5B
- MAGEL2
- MAOA
- MBD5
- MBOAT7
- MECP2
- MED12
- MED13
- MED13L
- MEF2C
- MET
- MYT1L
- NAA15
- NCKAP1
- NEXMIF
- NHS
- NIPBL
- NLGN3
- NLGN4X
- NRXN1
- NRXN3
- NSD1
- NTNG1
- OPHN1
- PAFAH1B1
- PAH
- PCDH19
- PDE4D
- PHF3
- PHIP
- POGZ
- PPM1D
- PPT1
- PQBP1
- PTCHD1
- PTEN
- PTPN11
- RAB39B
- RAI1
- RANBP17
- RELN
- RERE
- RIMS1
- RPL10
- SATB2
- SCN2A
- SCN8A
- SCN9A
- SEMA3E
- SEMA5A
- SETBP1
- SETD2
- SETD5
- SHANK2
- SHANK3
- SIN3A
- SLC6A1
- SLC6A8
- SLC9A6
- SLC9A9
- SMAD4
- SMARCC2
- SMC1A
- SMC3
- SOX5
- SPAST
- SRCAP
- SRSF11
- SYN1
- SYNGAP1
- TAOK2
- TBL1XR1
- TBR1
- TCF20
- TCF4
- TMLHE
- TNRC6B
- TRAPPC9
- TRIO
- TRIP12
- TSC1
- TSC2
- UBE3A
- UBN2
- UPF3B
- USP15
- USP7
- VPS13B
- WAC
- WDFY3
- WDR62
- ZBTB20
- ZEB2
- ZMYND11
EXOMAS
Raquitismo hipofosfatémico
Ref. 4011
12 genes
- ALPL
- CLCN5
- CYP27B1
- CYP2R1
- DMP1
- EHHADH
- ENPP1
- FGF23
- PHEX
- SLC34A1
- SLC34A3
- VDR
EXOMAS
Síndromes Aórticos
Ref. 4274
37 genes
- ACTA2
- B3GAT3
- COL1A1
- COL1A2
- COL3A1
- COL4A5
- COL5A1
- COL5A2
- EFEMP2
- ELN
- FBN1
- FBN2
- FLNA
- FOXE3
- GAA
- GATA5
- HRAS
- LOX
- MAT2A
- MED12
- MFAP5
- MYH11
- MYLK
- NKX2-5
- NOTCH1
- PLOD1
- PRKG1
- PTPN11
- SKI
- SLC2A10
- SMAD3
- SMAD4
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
- ZDHHC9
EXOMAS
Fibrilación Auricular Familiar
Ref. 3552
14 genes
- ABCC9
- GJA5
- KCNA5
- KCNE2
- KCNJ2
- KCNQ1
- MYL4
- NPPA
- NUP155
- SCN1B
- SCN2B
- SCN3B
- SCN4B
- SCN5A
EXOMAS
Distrofia Muscular de Cinturas
Ref. 4316
33 genes
- ANO5
- BVES
- CAPN3
- COL12A1
- COL6A1
- COL6A2
- COL6A3
- DAG1
- DNAJB6
- DYSF
- FKRP
- FKTN
- GMPPB
- HNRNPDL
- ISPD
- LAMA2
- LIMS2
- PLEC
- POGLUT1
- POMGNT1
- POMGNT2
- POMT1
- POMT2
- SGCA
- SGCB
- SGCD
- SGCG
- TCAP
- TNPO3
- TOR1AIP1
- TRAPPC11
- TRIM32
- TTN
EXOMAS
Hipoacusia Autosómica Recesiva
Ref. 4207
76 genes
- ADCY1
- ATP2B2
- BDP1
- BSND
- CABP2
- CDC14A
- CDH23
- CEACAM16
- CIB2
- CLDN14
- CLIC5
- COCH
- COL11A2
- DCDC2
- ELMOD3
- EPS8
- EPS8L2
- ESPN
- ESRP1
- ESRRB
- FOXI1
- GAB1
- GIPC3
- GJB2
- GJB3
- GJB6
- GPSM2
- GRXCR1
- GRXCR2
- HGF
- ILDR1
- KARS
- KCNJ10
- LHFPL5
- LOXHD1
- LRTOMT
- MARVELD2
- MET
- MPZL2
- MSRB3
- MYO15A
- MYO3A
- MYO6
- MYO7A
- NARS2
- OTOA
- OTOF
- OTOG
- OTOGL
- PCDH15
- PDZD7
- PJVK
- PNPT1
- PPIP5K2
- RDX
- RIPOR2
- ROR1
- S1PR2
- SERPINB6
- SLC22A4
- SLC26A4
- SLC26A5
- STRC
- SYNE4
- TBC1D24
- TECTA
- TMC1
- TMEM132E
- TMIE
- TMPRSS3
- TPRN
- TRIOBP
- TSPEAR
- USH1C
- WBP2
- WHRN
EXOMAS
Hipoacusia ligada a X
Ref. 4037
6 genes
- AIFM1
- COL4A6
- GPRASP2
- POU3F4
- PRPS1
- SMPX
EXOMAS
Neuropatía Motora Distal Hereditaria
Ref. 4587
29 genes
- ASAH1
- ASCC1
- ATP7A
- BSCL2
- CHCHD10
- DCTN1
- DNAJB2
- DYNC1H1
- FBXO38
- GARS
- HINT1
- HSPB1
- HSPB3
- HSPB8
- IGHMBP2
- PLEKHG5
- REEP1
- SCP2
- SETX
- SIGMAR1
- SLC52A3
- SLC5A2
- SLC5A7
- TFG
- TRPV4
- UBA1
- VAPB
- VRK1
- WARS
EXOMAS
Neuropatías
Ref. 4588
106 genes
- AARS
- ABHD12
- AIFM1
- ARHGEF10
- ASAH1
- ASCC1
- ATL1
- ATL3
- ATP1A1
- ATP7A
- BAG3
- BSCL2
- CHCHD10
- CNTNAP1
- COA7
- COX6A1
- DCAF8
- DCTN1
- DCTN2
- DGAT2
- DHTKD1
- DNAJB2
- DNM2
- DNMT1
- DRP2
- DST
- DYNC1H1
- EGR2
- ELP1
- FBXO38
- FGD4
- FIG4
- GARS
- GDAP1
- GJB1
- GJB3
- GNB4
- HARS
- HINT1
- HK1
- HSPB1
- HSPB3
- HSPB8
- IGHMBP2
- INF2
- JPH1
- KARS
- KIF1A
- KIF1B
- KIF5A
- LITAF
- LMNA
- LRSAM1
- MARS
- MCM3AP
- MED25
- MFN2
- MME
- MORC2
- MPV17
- MPZ
- MTMR2
- NAGLU
- NDRG1
- NEFH
- NEFL
- NGF
- NTRK1
- PDK3
- PLEKHG5
- PMP2
- PMP22
- PRDM12
- PRPS1
- PRX
- RAB7A
- REEP1
- RETREG1
- SBF1
- SBF2
- SCN11A
- SCN9A
- SCO2
- SCP2
- SETX
- SGPL1
- SH3TC2
- SIGMAR1
- SLC52A3
- SLC5A2
- SLC5A7
- SPG11
- SPTLC1
- SPTLC2
- SURF1
- SYT2
- TFG
- TRIM2
- TRPV4
- UBA1
- VAPB
- VCP
- VRK1
- WARS
- WNK1
- YARS
EXOMAS
Neuropatías
Ref. 4272
97 genes
- AARS
- ABHD12
- AIFM1
- ARHGEF10
- ATL1
- ATL3
- ATP1A1
- ATP7A
- BAG3
- BSCL2
- CNTNAP1
- COA7
- COX6A1
- DCAF8
- DCTN1
- DCTN2
- DGAT2
- DHTKD1
- DNAJB2
- DNM2
- DNMT1
- DRP2
- DST
- DYNC1H1
- EGR2
- ELP1
- FBXO38
- FGD4
- FIG4
- GARS
- GDAP1
- GJB1
- GJB3
- GNB4
- HARS
- HINT1
- HK1
- HSPB1
- HSPB3
- HSPB8
- IGHMBP2
- INF2
- JPH1
- KARS
- KIF1A
- KIF1B
- KIF5A
- LITAF
- LMNA
- LRSAM1
- MARS
- MCM3AP
- MED25
- MFN2
- MME
- MORC2
- MPV17
- MPZ
- MTMR2
- NAGLU
- NDRG1
- NEFH
- NEFL
- NGF
- NTRK1
- PDK3
- PLEKHG5
- PMP2
- PMP22
- PRDM12
- PRPS1
- PRX
- RAB7A
- REEP1
- RETREG1
- SBF1
- SBF2
- SCN11A
- SCN9A
- SCO2
- SETX
- SGPL1
- SH3TC2
- SIGMAR1
- SLC5A7
- SPG11
- SPTLC1
- SPTLC2
- SURF1
- SYT2
- TFG
- TRIM2
- TRPV4
- VCP
- WARS
- WNK1
- YARS
EXOMAS
Charcot-Marie-Tooth Desmielinizante
Ref. 4262
26 genes
- ABHD12
- AIFM1
- ARHGEF10
- CNTNAP1
- EGR2
- FGD4
- FIG4
- GDAP1
- GJB1
- HARS
- HK1
- LITAF
- MCM3AP
- MPZ
- MTMR2
- NDRG1
- NEFL
- PDK3
- PMP2
- PMP22
- PRPS1
- PRX
- SBF1
- SBF2
- SH3TC2
- SURF1
EXOMAS
Charcot-Marie-Tooth Intermedio
Ref. 4268
13 genes
- COX6A1
- DNM2
- DRP2
- GDAP1
- GJB1
- GNB4
- INF2
- KARS
- MPZ
- NEFL
- PLEKHG5
- PRPS1
- YARS
EXOMAS
Distrofias de retina
Ref. 4580
198 genes
- ABCA4
- ABCC6
- ABHD12
- ADAM9
- ADAMTS18
- ADGRA3
- ADGRV1
- AGBL5
- AHR
- AIPL1
- ALMS1
- APOE
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- ARMS2
- ATF6
- BBS1
- BBS2
- BBS4
- BEST1
- C1QTNF5
- C2
- C3
- C8orf37
- C9
- CA4
- CABP4
- CACNA1F
- CACNA2D4
- CDH23
- CDH3
- CDHR1
- CEP250
- CEP290
- CEP78
- CERKL
- CFAP410
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CIB2
- CLN3
- CLRN1
- CLUAP1
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- CNNM4
- CRB1
- CRX
- CST3
- CTNNA1
- CWC27
- CX3CR1
- CYP4V2
- DHDDS
- DHX38
- DNAJC17
- DRAM2
- DTHD1
- EFEMP1
- ELOVL4
- EMC1
- ERCC6
- EYS
- FAM161A
- FBLN5
- FLVCR1
- FSCN2
- GDF6
- GNAT2
- GRK1
- GRM6
- GUCA1A
- GUCA1B
- GUCY2D
- HGSNAT
- HK1
- HMCN1
- HTRA1
- IDH3A
- IDH3B
- IFT140
- IFT172
- IFT43
- IFT81
- IMPDH1
- IMPG1
- IMPG2
- INPP5E
- IQCB1
- KCNJ13
- KCNV2
- KIAA1549
- KIZ
- KLHL7
- LARGE2
- LCA5
- LRAT
- LRIT3
- MAK
- MAPKAPK3
- MERTK
- MFRP
- MVK
- MYO7A
- NEK2
- NEUROD1
- NMNAT1
- NR2E3
- NRL
- NYX
- OAT
- OFD1
- OPN1LW
- OPN1SW
- OTX2
- PANK2
- PCARE
- PDE6A
- PDE6B
- PDE6C
- PDE6G
- PDE6H
- PEX1
- PEX2
- PEX7
- PHYH
- PITPNM3
- PLA2G5
- POC1B
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RAB28
- RAX2
- RBP3
- RBP4
- RD3
- RDH12
- RDH5
- REEP6
- RGR
- RGS9
- RGS9BP
- RHO
- RIMS1
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- RPGRIP1
- RS1
- SAG
- SAMD11
- SCAPER
- SCLT1
- SEMA4A
- SEMA6B
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TEAD1
- TIMP1
- TIMP3
- TLR3
- TLR4
- TOPORS
- TRNT1
- TTC8
- TTLL5
- TTPA
- TUB
- TULP1
- UNC119
- USH1C
- USH1G
- USH2A
- VPS13B
- WDR19
- WHRN
- ZNF408
- ZNF513
EXOMAS
Distrofias de retina
Ref. 4299
159 genes
- ABCA4
- ABCC6
- ADAM9
- ADGRA3
- AGBL5
- AHR
- AIPL1
- ALMS1
- APOE
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- ARMS2
- ATF6
- BBS1
- BBS2
- BEST1
- C1QTNF5
- C2
- C3
- C8orf37
- C9
- CA4
- CABP4
- CACNA1F
- CACNA2D4
- CDH3
- CDHR1
- CEP290
- CEP78
- CERKL
- CFAP410
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CLRN1
- CLUAP1
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- CNNM4
- CRB1
- CRX
- CST3
- CTNNA1
- CX3CR1
- CYP4V2
- DHDDS
- DHX38
- DRAM2
- DTHD1
- EFEMP1
- ELOVL4
- EMC1
- ERCC6
- EYS
- FAM161A
- FBLN5
- FSCN2
- GDF6
- GNAT2
- GUCA1A
- GUCA1B
- GUCY2D
- HGSNAT
- HK1
- HMCN1
- HTRA1
- IDH3B
- IFT140
- IFT172
- IFT43
- IFT81
- IMPDH1
- IMPG1
- IMPG2
- IQCB1
- KCNJ13
- KCNV2
- KIAA1549
- KIZ
- KLHL7
- LCA5
- LRAT
- MAK
- MAPKAPK3
- MERTK
- MVK
- NEK2
- NEUROD1
- NMNAT1
- NR2E3
- NRL
- OFD1
- OPN1LW
- OPN1MW
- OTX2
- PCARE
- PDE6A
- PDE6B
- PDE6C
- PDE6G
- PDE6H
- PITPNM3
- POC1B
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RAB28
- RAX2
- RBP3
- RBP4
- RD3
- RDH12
- RDH5
- REEP6
- RGR
- RGS9
- RGS9BP
- RHO
- RIMS1
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- RPGRIP1
- RS1
- SAG
- SEMA4A
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TEAD1
- TIMP3
- TLR3
- TLR4
- TOPORS
- TRNT1
- TTC8
- TTLL5
- TULP1
- UNC119
- USH2A
- ZNF408
- ZNF513
EXOMAS
Distrofias de retina
Ref. 4656
160 genes
- ABCA4
- ABCC6
- ADAM9
- ADGRA3
- AGBL5
- AHR
- AIPL1
- ALMS1
- APOE
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- ARMS2
- ATF6
- BBS1
- BBS2
- BEST1
- C1QTNF5
- C2
- C3
- C8orf37
- C9
- CA4
- CABP4
- CACNA1F
- CACNA2D4
- CDH3
- CDHR1
- CEP290
- CEP78
- CERKL
- CFAP410
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CHM
- CLRN1
- CLUAP1
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- CNNM4
- CRB1
- CRX
- CST3
- CTNNA1
- CX3CR1
- CYP4V2
- DHDDS
- DHX38
- DRAM2
- DTHD1
- EFEMP1
- ELOVL4
- EMC1
- ERCC6
- EYS
- FAM161A
- FBLN5
- FSCN2
- GDF6
- GNAT2
- GUCA1A
- GUCA1B
- GUCY2D
- HGSNAT
- HK1
- HMCN1
- HTRA1
- IDH3B
- IFT140
- IFT172
- IFT43
- IFT81
- IMPDH1
- IMPG1
- IMPG2
- IQCB1
- KCNJ13
- KCNV2
- KIAA1549
- KIZ
- KLHL7
- LCA5
- LRAT
- MAK
- MAPKAPK3
- MERTK
- MVK
- NEK2
- NEUROD1
- NMNAT1
- NR2E3
- NRL
- OFD1
- OPN1LW
- OPN1MW
- OTX2
- PCARE
- PDE6A
- PDE6B
- PDE6C
- PDE6G
- PDE6H
- PITPNM3
- POC1B
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RAB28
- RAX2
- RBP3
- RBP4
- RD3
- RDH12
- RDH5
- REEP6
- RGR
- RGS9
- RGS9BP
- RHO
- RIMS1
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- RPGRIP1
- RS1
- SAG
- SEMA4A
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TEAD1
- TIMP3
- TLR3
- TLR4
- TOPORS
- TRNT1
- TTC8
- TTLL5
- TULP1
- UNC119
- USH2A
- ZNF408
- ZNF513
EXOMAS
Distrofias de retina
Ref. 4714
211 genes
- ABCA4
- ACO2
- ADAM9
- ADGRA3
- AGBL5
- AGK
- AHR
- AIPL1
- ALMS1
- APOE
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- ARMS2
- ASB10
- ATF6
- BBS1
- BBS2
- BEST1
- BFSP1
- BFSP2
- C2
- C3
- C8orf37
- C9
- CA4
- CABP4
- CACNA1F
- CACNA2D4
- CDHR1
- CEP290
- CEP78
- CERKL
- CFAP410
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CHM
- CHMP4B
- CLRN1
- CLUAP1
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- CNNM4
- CRB1
- CRX
- CRYAA
- CRYAB
- CRYBA1
- CRYBA2
- CRYBA4
- CRYBB1
- CRYBB2
- CRYBB3
- CRYGB
- CRYGC
- CRYGD
- CRYGS
- CST3
- CTNNA1
- CX3CR1
- CYP1B1
- CYP4V2
- DHDDS
- DHX38
- DNM1L
- DRAM2
- DTHD1
- EFEMP1
- ELOVL4
- EMC1
- EPHA2
- ERCC6
- EYS
- FAM161A
- FBLN5
- FOXE3
- FSCN2
- FYCO1
- GCNT2
- GDF6
- GJA3
- GJA8
- GNAT1
- GNAT2
- GNB3
- GPR179
- GRK1
- GRM6
- GUCA1A
- GUCA1B
- GUCY2D
- HGSNAT
- HK1
- HMCN1
- HSF4
- HTRA1
- IDH3B
- IFT140
- IFT172
- IFT43
- IFT81
- IMPDH1
- IMPG1
- IMPG2
- IQCB1
- KCNJ13
- KCNV2
- KIAA1549
- KIZ
- KLHL7
- LCA5
- LEMD2
- LIM2
- LRAT
- LRIT3
- LSS
- LTBP2
- MAF
- MAK
- MERTK
- MIP
- MVK
- MYOC
- NEK2
- NEUROD1
- NHS
- NMNAT1
- NR2E3
- NRL
- NTF4
- NYX
- OFD1
- OPA1
- OPA3
- OPN1LW
- OPN1MW
- OPN1SW
- OPTN
- OTX2
- PCARE
- PDE6A
- PDE6B
- PDE6C
- PDE6G
- PDE6H
- PITPNM3
- PITX3
- POC1B
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RAB28
- RAX2
- RBP3
- RD3
- RDH12
- RDH5
- REEP6
- RGR
- RHO
- RIMS1
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- RPGRIP1
- RS1
- RTN4IP1
- SAG
- SEMA4A
- SIPA1L3
- SLC24A1
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TBK1
- TDRD7
- TEK
- TIMP3
- TMEM126A
- TOPORS
- TRNT1
- TRPM1
- TTC8
- TTLL5
- TULP1
- UNC119
- UNC45B
- USH2A
- VIM
- WDR36
- WFS1
- YME1L1
- ZNF408
- ZNF513
EXOMAS
Distrofias de retina
Ref. 10056
160 genes
- ABCA4
- ADAM9
- ADGRA3
- AGBL5
- AHR
- AIPL1
- ALMS1
- APOE
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- ARMS2
- ATF6
- BBS1
- BBS2
- BEST1
- C2
- C3
- C8orf37
- C9
- CA4
- CABP4
- CACNA1F
- CACNA2D4
- CDHR1
- CEP290
- CEP78
- CERKL
- CFAP410
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CHM
- CLRN1
- CLUAP1
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- CNNM4
- CRB1
- CRX
- CST3
- CTNNA1
- CX3CR1
- CYP4V2
- DHDDS
- DHX38
- DRAM2
- DTHD1
- EFEMP1
- ELOVL4
- EMC1
- ERCC6
- EYS
- FAM161A
- FBLN5
- FSCN2
- GDF6
- GNAT1
- GNAT2
- GNB3
- GPR179
- GRK1
- GRM6
- GUCA1A
- GUCA1B
- GUCY2D
- HGSNAT
- HK1
- HMCN1
- HTRA1
- IDH3B
- IFT140
- IFT172
- IFT43
- IFT81
- IMPDH1
- IMPG1
- IMPG2
- IQCB1
- KCNJ13
- KCNV2
- KIAA1549
- KIZ
- KLHL7
- LCA5
- LRAT
- LRIT3
- MAK
- MERTK
- MVK
- NEK2
- NEUROD1
- NMNAT1
- NR2E3
- NRL
- NYX
- OFD1
- OPN1LW
- OPN1MW
- OPN1SW
- OTX2
- PCARE
- PDE6A
- PDE6B
- PDE6C
- PDE6G
- PDE6H
- PITPNM3
- POC1B
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RAB28
- RAX2
- RBP3
- RD3
- RDH12
- RDH5
- REEP6
- RGR
- RHO
- RIMS1
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- RPGRIP1
- RS1
- SAG
- SEMA4A
- SLC24A1
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TIMP3
- TOPORS
- TRNT1
- TRPM1
- TTC8
- TTLL5
- TULP1
- UNC119
- USH2A
- ZNF408
- ZNF513
EXOMAS
Retinosis Pigmentaria
Ref. 4513
62 genes
- ABCA4
- AGBL5
- AHI1
- ARHGEF18
- ARL2BP
- ARL6
- BBS2
- BEST1
- C8orf37
- CA4
- CDHR1
- CERKL
- CLRN1
- CNGA1
- CNGB1
- CRB1
- CRX
- DHDDS
- EYS
- FAM161A
- FSCN2
- GUCA1B
- HGSNAT
- IDH3B
- IFT140
- IFT172
- IMPDH1
- IMPG2
- KIZ
- KLHL7
- LRAT
- MAK
- MERTK
- NEK2
- NR2E3
- NRL
- OFD1
- PCARE
- PDE6A
- PDE6B
- PDE6G
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RBP3
- RDH12
- REEP6
- RGR
- RHO
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
EXOMAS
Retinosis Pigmentaria
Ref. 4291
87 genes
- ABCA4
- ADGRA3
- AGBL5
- AHR
- AIPL1
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- BBS1
- BBS2
- BEST1
- C8orf37
- CA4
- CDHR1
- CERKL
- CLRN1
- CNGA1
- CNGB1
- CRB1
- CRX
- CYP4V2
- DHDDS
- DHX38
- EMC1
- EYS
- FAM161A
- FSCN2
- GUCA1B
- HGSNAT
- HK1
- IDH3B
- IFT140
- IFT172
- IFT43
- IMPDH1
- IMPG2
- KIAA1549
- KIZ
- KLHL7
- LRAT
- MAK
- MERTK
- MVK
- NEK2
- NEUROD1
- NR2E3
- NRL
- OFD1
- PCARE
- PDE6A
- PDE6B
- PDE6G
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RBP3
- RDH12
- REEP6
- RGR
- RHO
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- SAG
- SEMA4A
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TOPORS
- TRNT1
- TTC8
- TULP1
- USH2A
- ZNF408
- ZNF513
EXOMAS
Retinosis Pigmentaria
Ref. 4657
88 genes
- ABCA4
- ADGRA3
- AGBL5
- AHR
- AIPL1
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- BBS1
- BBS2
- BEST1
- C8orf37
- CA4
- CDHR1
- CERKL
- CHM
- CLRN1
- CNGA1
- CNGB1
- CRB1
- CRX
- CYP4V2
- DHDDS
- DHX38
- EMC1
- EYS
- FAM161A
- FSCN2
- GUCA1B
- HGSNAT
- HK1
- IDH3B
- IFT140
- IFT172
- IFT43
- IMPDH1
- IMPG2
- KIAA1549
- KIZ
- KLHL7
- LRAT
- MAK
- MERTK
- MVK
- NEK2
- NEUROD1
- NR2E3
- NRL
- OFD1
- PCARE
- PDE6A
- PDE6B
- PDE6G
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RBP3
- RDH12
- REEP6
- RGR
- RHO
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- SAG
- SEMA4A
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TOPORS
- TRNT1
- TTC8
- TULP1
- USH2A
- ZNF408
- ZNF513
EXOMAS
Distrofia de Conos y Bastones
Ref. 4290
43 genes
- ABCA4
- ADAM9
- AIPL1
- ATF6
- C8orf37
- CABP4
- CACNA1F
- CACNA2D4
- CDHR1
- CEP78
- CERKL
- CFAP410
- CNGA3
- CNGB3
- CNNM4
- CRB1
- CRX
- DRAM2
- ELOVL4
- EYS
- GNAT2
- GUCA1A
- GUCY2D
- IFT81
- KCNV2
- OPN1LW
- OPN1MW
- PDE6C
- PDE6H
- PITPNM3
- POC1B
- PROM1
- PRPH2
- RAB28
- RAX2
- RDH5
- RIMS1
- RPGR
- RPGRIP1
- SEMA4A
- TTLL5
- TULP1
- UNC119
EXOMAS
Degeneración Macular Asociada a la Edad
Ref. 4288
18 genes
- ABCA4
- APOE
- ARMS2
- C2
- C3
- C9
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CST3
- CX3CR1
- ERCC6
- FBLN5
- HMCN1
- HTRA1
- RAX2
EXOMAS
Taquicardia Ventricular Polimórfica Catecolinérgica
Ref. 10010
6 genes
- CALM1
- CALM3
- CASQ2
- RYR2
- TECRL
- TRDN
EXOMAS
Taquicardia Ventricular Polimórfica Catecolinérgica
Ref. 4257
5 genes
- CALM1
- CASQ2
- RYR2
- TECRL
- TRDN
EXOMAS
Meckel, síndrome
Ref. 3595
13 genes
- B9D1
- B9D2
- CC2D2A
- CEP290
- KIF14
- MKS1
- NPHP3
- RPGRIP1L
- TCTN2
- TMEM107
- TMEM216
- TMEM231
- TMEM67
EXOMAS
Nefronoptisis
Ref. 4048
21 genes
- ANKS6
- CEP164
- CEP290
- CEP83
- DCDC2
- GLIS2
- IFT172
- INVS
- IQCB1
- MAPKBP1
- NEK8
- NPHP1
- NPHP3
- NPHP4
- RPGRIP1L
- SDCCAG8
- TMEM67
- TTC21B
- WDR19
- XPNPEP3
- ZNF423
EXOMAS
Poliquistosis Renal
Ref. 3902
6 genes
- DNAJB11
- DZIP1L
- GANAB
- PKD1
- PKD2
- PKHD1
EXOMAS
Síndrome Nefrótico Resistente a Esteroides
Ref. 4047
56 genes
- ACTN4
- ALG1
- ANLN
- APOL1
- ARHGAP24
- ARHGDIA
- CD151
- CD2AP
- CFH
- COL4A3
- COL4A4
- COL4A5
- COQ2
- COQ6
- COQ8B
- CRB2
- CUBN
- DGKE
- E2F3
- EMP2
- FAT1
- GPC5
- INF2
- ITGA3
- ITGB4
- KANK1
- KANK2
- KANK4
- LAMB2
- LMNA
- LMX1B
- MAGI2
- MYH9
- MYO1E
- NPHS1
- NPHS2
- NUP107
- NUP205
- NUP93
- NXF5
- OCRL
- PAX2
- PDSS2
- PLCE1
- PMM2
- PODXL
- PTPRO
- SCARB2
- SMARCAL1
- SYNPO
- TRPC6
- TTC21B
- WDR73
- WT1
- XPO5
- ZMPSTE24
EXOMAS
Ataxia Espinocerebelosa
Ref. 4306
55 genes
- AFG3L2
- ANO10
- ATN1
- ATP1A3
- BEAN1
- C9orf72
- CACNA1A
- CACNA1G
- CCDC88C
- COQ8A
- CWF19L1
- DAB1
- DNMT1
- EEF2
- ELOVL4
- ELOVL5
- FAT2
- FGF12
- FGF14
- GRID2
- GRM1
- ITPR1
- KCNC3
- KCND3
- MME
- NOP56
- PDYN
- PLD3
- PMPCA
- POLG
- PPP2R2B
- PRKCG
- PUM1
- RUBCN
- SCYL1
- SLC9A1
- SNX14
- SPTBN2
- STUB1
- SYT14
- TBP
- TDP1
- TDP2
- TGM6
- TMEM240
- TPP1
- TRPC3
- TTBK2
- TUBB4A
- TWNK
- UBA5
- VPS13D
- VWA3B
- WDR73
- WWOX
EXOMAS
Ataxia con Espasticidad
Ref. 4307
9 genes
- AFG3L2
- CHP1
- KIF1C
- MARS2
- MTPAP
- NKX6-2
- SACS
- SPG7
- VAMP1
EXOMAS
Fahr, enfermedad
Ref. 3666
4 genes
- PDGFB
- PDGFRB
- SLC20A2
- XPR1
EXOMAS
Temblor esencial
Ref. 3616
3 genes
- DRD3
- FUS
- TENM4
EXOMAS
Discapacidad Intelectual Autosómica Dominante
Ref. 3705
59 genes
- ADNP
- AHDC1
- ARID1A
- ARID1B
- ARID2
- ASH1L
- AUTS2
- CACNG2
- CAMK2A
- CAMK2B
- CDH15
- CHAMP1
- CIC
- CLTC
- COL4A3BP
- CTCF
- CTNNB1
- DEAF1
- DOCK8
- DPP6
- DYNC1H1
- DYRK1A
- EEF1A2
- EHMT1
- EPB41L1
- GATAD2B
- GNB1
- GRIN2B
- HIVEP2
- KANSL1
- KAT6A
- KCNQ5
- KIF1A
- KIRREL3
- KMT5B
- MBD5
- MEF2C
- MYT1L
- NAA15
- NUS1
- PACS1
- POGZ
- PPP2R1A
- PPP2R5D
- PURA
- RAC1
- SETBP1
- SETD5
- SMARCA4
- SMARCB1
- SMARCE1
- SOX11
- STAG1
- SYNGAP1
- TBL1XR1
- TRIO
- TRIP12
- ZBTB18
- ZMYND11
EXOMAS
Discapacidad Intelectual Autosómica Recesiva
Ref. 3706
40 genes
- ADAT3
- ANK3
- CC2D1A
- CRADD
- CRBN
- EDC3
- ELP2
- FBXO31
- FMN2
- GPT2
- GRIK2
- HERC2
- HNMT
- IMPA1
- KPTN
- LINS1
- LMAN2L
- MAN1B1
- MBOAT7
- MED23
- METTL23
- NDST1
- NSUN2
- PGAP1
- PIGC
- PIGG
- PRSS12
- PUS3
- RUSC2
- SLC6A17
- ST3GAL3
- TAF13
- TAF2
- TECR
- TNIK
- TRAPPC9
- TTI2
- TUSC3
- WASHC4
- ZC3H14
EXOMAS
Paraplejia Espástica Autosómica Dominante
Ref. 4303
23 genes
- ADAR
- ALDH18A1
- ATAD3A
- ATL1
- ATP2B4
- BICD2
- BSCL2
- CPT1C
- DNM2
- ERLIN2
- HSPD1
- KIF5A
- NIPA1
- REEP1
- REEP2
- RTN2
- SLC33A1
- SPAST
- SPG7
- TUBB4A
- UBAP1
- WASHC5
- ZFYVE27
EXOMAS
Paraplejia Espástica Autosómica Recesiva
Ref. 3975
52 genes
- ALDH18A1
- ALDH3A2
- AMPD2
- AP4B1
- AP4E1
- AP4M1
- AP4S1
- AP5Z1
- ARL6IP1
- ATL1
- ATP13A2
- B4GALNT1
- BICD2
- C12orf65
- C19orf12
- CAPN1
- CYP2U1
- CYP7B1
- DDHD1
- DDHD2
- DSTYK
- ENTPD1
- ERLIN1
- ERLIN2
- FA2H
- FARS2
- GAD1
- GBA2
- GJC2
- GRID2
- IBA57
- KIF1A
- KIF1C
- KLC2
- KLC4
- MAG
- MARS
- NT5C2
- PGAP1
- PNPLA6
- REEP2
- SPART
- SPG11
- SPG21
- SPG7
- TECPR2
- TFG
- UCHL1
- USP8
- VPS37A
- WDR48
- ZFYVE26
EXOMAS
Distroglicanopatías
Ref. 4590
14 genes
- B3GALNT2
- B4GAT1
- DAG1
- FKRP
- FKTN
- GMPPB
- ISPD
- LARGE1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
EXOMAS
Distroglicanopatías
Ref. 4591
14 genes
- B3GALNT2
- B4GAT1
- DAG1
- FKRP
- FKTN
- GMPPB
- ISPD
- LARGE1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
EXOMAS
Distroglicanopatías
Ref. 4592
14 genes
- B3GALNT2
- B4GAT1
- DAG1
- FKRP
- FKTN
- GMPPB
- ISPD
- LARGE1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
EXOMAS
Distroglicanopatías
Ref. 4593
14 genes
- B3GALNT2
- B4GAT1
- DAG1
- FKRP
- FKTN
- GMPPB
- ISPD
- LARGE1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
EXOMAS
Distroglicanopatías
Ref. 4594
14 genes
- B3GALNT2
- B4GAT1
- DAG1
- FKRP
- FKTN
- GMPPB
- ISPD
- LARGE1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
EXOMAS
Distroglicanopatías
Ref. 4595
14 genes
- B3GALNT2
- B4GAT1
- DAG1
- FKRP
- FKTN
- GMPPB
- ISPD
- LARGE1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
EXOMAS
Miopatías Distales
Ref. 4605
26 genes
- ADSSL1
- AGL
- ANO5
- BAG3
- CAV3
- CRYAB
- DES
- DNAJB6
- DNM2
- DYSF
- FLNC
- GNE
- KY
- LDB3
- LMNA
- MATR3
- MMD2
- MYH7
- MYOT
- PNPLA2
- PYROXD1
- SQSTM1
- TIA1
- TRPV4
- TTN
- VCP
EXOMAS
Defectos del sistema OXPHOS
Ref. 3684
55 genes
- ABCB7
- ATPAF2
- BCS1L
- COQ2
- COQ8A
- COX10
- COX15
- COX6B1
- DARS2
- DNAJC19
- DNM1L
- FXN
- GFM1
- GLRX5
- HSPD1
- ISCU
- LETM1
- LRPPRC
- MFN2
- MRPS16
- MRPS22
- NDUFA1
- NDUFA11
- NDUFA2
- NDUFAF1
- NDUFAF2
- NDUFAF4
- NDUFAF6
- NDUFS1
- NDUFS2
- NDUFS3
- NDUFS4
- NDUFS6
- NDUFS7
- NDUFS8
- NDUFV1
- NDUFV2
- OPA1
- PDSS1
- PDSS2
- PUS1
- SCO1
- SCO2
- SDHA
- SDHB
- SDHC
- SDHD
- SPG7
- SURF1
- TAZ
- TIMM8A
- TSFM
- TUFM
- UQCRB
- UQCRQ
EXOMAS
Deficiencia de la Coenzima Q10
Ref. 4518
9 genes
- COQ2
- COQ4
- COQ6
- COQ7
- COQ8A
- COQ8B
- COQ9
- PDSS1
- PDSS2
EXOMAS
Demencia Frontotemporal
Ref. 3686
8 genes
- C9orf72
- CHMP2B
- FUS
- GRN
- MAPT
- PSEN1
- TARDBP
- VCP
EXOMAS
Epilepsia Mioclónica Progresiva
Ref. 3689
11 genes
- CERS1
- CSTB
- EPM2A
- GOSR2
- KCNC1
- KCTD7
- LMNB2
- NHLRC1
- PRDM8
- PRICKLE1
- SCARB2
EXOMAS
Leucodistrofia Hipomielinizante
Ref. 4524
18 genes
- AIMP1
- AIMP2
- DEGS1
- EPRS
- FAM126A
- GJC2
- HIKESHI
- HSPD1
- PLP1
- POLR1C
- POLR3A
- POLR3B
- PYCR2
- RARS
- TMEM106B
- TUBB4A
- UFM1
- VPS11
EXOMAS
Megalencefalia-Polimicrogiria y Megalencefalia Displásica
Ref. 3696
7 genes
- AKT3
- DEPDC5
- EZH2
- MTOR
- NPRL3
- PIK3CA
- PIK3R2
EXOMAS
Displasias Corticales
Ref. 3697
57 genes
- ACTB
- ACTG1
- ADGRG1
- AKT3
- ARFGEF2
- ARX
- CDK5
- CHD7
- COL18A1
- DCHS1
- DCX
- DEPDC5
- DYNC1H1
- EOMES
- ERMARD
- EZH2
- FAT4
- FH
- FIG4
- FKRP
- FKTN
- FLNA
- FMR1
- KATNB1
- KIF1BP
- KIF2A
- KIF5C
- LAMB1
- LARGE1
- LRP2
- MTOR
- NDE1
- NPRL3
- NSDHL
- OCLN
- PAFAH1B1
- PAX6
- PIK3CA
- PIK3R2
- POMGNT1
- POMT1
- POMT2
- RAB18
- RAB3GAP1
- RAB3GAP2
- RELN
- RTTN
- SNAP29
- SRPX2
- TMTC3
- TUBA1A
- TUBA8
- TUBB2B
- TUBB3
- TUBG1
- VLDLR
- WDR62
EXOMAS
Rett-like, síndrome
Ref. 3929
41 genes
- ARX
- BTBD9
- CACNA1I
- CDKL5
- CHD4
- CHRNA5
- CNTNAP2
- EEF1A2
- EIF2B2
- FOXG1
- FOXP2
- GABBR2
- GRIN2A
- GRIN2B
- HCN1
- HERC2
- IQSEC2
- KCNA2
- KCNQ2
- MECP2
- MEF2C
- NRXN1
- NTNG1
- PLP1
- SCN1A
- SCN2A
- SCN8A
- SHANK3
- SHROOM4
- SLC2A1
- SLC39A13
- SLC6A1
- SMC1A
- STXBP1
- SYNGAP1
- TBL1XR1
- TCF4
- UBE3A
- WDR45
- ZBTB18
- ZEB2
EXOMAS
Aicardi-Goutieres, síndrome
Ref. 3700
7 genes
- ADAR
- IFIH1
- RNASEH2A
- RNASEH2B
- RNASEH2C
- SAMHD1
- TREX1
EXOMAS
Distrofia Muscular Congénita
Ref. 4589
75 genes
- ACTA1
- AGRN
- ALG13
- ANO5
- B3GALNT2
- B3GNT2
- B4GAT1
- BVES
- CAPN3
- CAV3
- CAVIN1
- CHKB
- COL12A1
- COL6A1
- COL6A2
- COL6A3
- DAG1
- DES
- DMD
- DNAJB6
- DOK7
- DOLK
- DPAGT1
- DPM1
- DPM2
- DPM3
- DYSF
- EMD
- FAT1
- FHL1
- FKRP
- FKTN
- FLNC
- GFPT1
- GMPPB
- HNRNPDL
- INPP5K
- ISPD
- ITGA7
- ITGA9
- KLHL9
- LAMA2
- LARGE1
- LIMS2
- LMNA
- MEGF10
- MICU1
- MYOT
- PABPN1
- PLEC
- POGLUT1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
- RYR1
- SELENON
- SGCA
- SGCB
- SGCD
- SGCG
- SMCHD1
- STIM1
- SYNE1
- SYNE2
- TCAP
- TMEM43
- TNPO3
- TOR1AIP1
- TRAPPC11
- TRIM32
- TRIP4
- TTN
EXOMAS
Distrofia Muscular Congénita
Ref. 3959
71 genes
- AGRN
- ALG13
- ANO5
- B3GALNT2
- B4GAT1
- BVES
- CAPN3
- CAV3
- CAVIN1
- CHKB
- COL12A1
- COL6A1
- COL6A2
- COL6A3
- DAG1
- DES
- DMD
- DNAJB6
- DOK7
- DOLK
- DPAGT1
- DPM1
- DPM2
- DPM3
- DYSF
- EMD
- FAT1
- FHL1
- FKRP
- FKTN
- FLNC
- GFPT1
- GMPPB
- HNRNPDL
- ISPD
- ITGA7
- ITGA9
- KLHL9
- LAMA2
- LARGE1
- LIMS2
- LMNA
- MEGF10
- MICU1
- MYOT
- PABPN1
- PLEC
- POGLUT1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
- RYR1
- SELENON
- SGCA
- SGCB
- SGCD
- SGCG
- SMCHD1
- STIM1
- SYNE1
- SYNE2
- TCAP
- TMEM43
- TNPO3
- TOR1AIP1
- TRAPPC11
- TRIM32
- TTN
EXOMAS
Hipoplasia Pontocerebelosa
Ref. 4313
18 genes
- AMPD2
- CHMP1A
- CLP1
- COASY
- EXOSC3
- EXOSC8
- EXOSC9
- PCLO
- RARS2
- SEPSECS
- TBC1D23
- TOE1
- TSEN15
- TSEN2
- TSEN34
- TSEN54
- VPS53
- VRK1
EXOMAS
Discapacidad Intelectual y Autismo
Ref. 4045
866 genes
- AAAS
- AASS
- ABAT
- ABCD1
- ABHD5
- ACADS
- ACHE
- ACO2
- ACOX1
- ACSF3
- ACSL4
- ACTB
- ACTG1
- ACY1
- ADAMTSL2
- ADAR
- ADAT3
- ADCY3
- ADCY5
- ADD3
- ADGRG1
- ADK
- ADNP
- ADRA2B
- ADSL
- AFF2
- AFF4
- AGA
- AGTR2
- AHDC1
- AHI1
- AIMP1
- AKAP9
- AKT3
- ALDH18A1
- ALDH3A2
- ALDH4A1
- ALDH5A1
- ALDH7A1
- ALDOA
- ALG1
- ALG11
- ALG12
- ALG13
- ALG2
- ALG3
- ALG6
- ALG9
- ALX3
- ALX4
- AMPD2
- AMT
- ANK2
- ANK3
- ANKRD11
- ANTXR1
- AP1S2
- AP3B1
- AP4B1
- AP4E1
- AP4M1
- AP4S1
- APH1A
- APOPT1
- APTX
- ARFGEF2
- ARG1
- ARHGEF6
- ARHGEF9
- ARID1A
- ARID1B
- ARID2
- ARL13B
- ARL6
- ARNT2
- ARX
- ASCL1
- ASH1L
- ASL
- ASNS
- ASPA
- ASPM
- ASS1
- ASXL1
- ASXL3
- ATIC
- ATP10A
- ATP1A2
- ATP2A2
- ATP6AP2
- ATP6V0A2
- ATP7A
- ATP8A2
- ATR
- ATRX
- AUH
- AUTS2
- AVPR1A
- B3GALNT2
- B3GLCT
- B4GALT1
- BAZ2B
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- BCKDHA
- BCKDHB
- BCKDK
- BCL11A
- BCOR
- BCS1L
- BLM
- BMPER
- BRAF
- BRF1
- BRWD3
- BSCL2
- BSND
- BTD
- BUB1B
- C12orf57
- C12orf65
- C2CD3
- CA2
- CA8
- CACNA1A
- CACNA1C
- CACNA1D
- CACNA1G
- CACNA1H
- CACNA2D3
- CACNG2
- CAMK2A
- CAMK2B
- CAMTA1
- CASK
- CBL
- CBS
- CC2D1A
- CC2D2A
- CCDC22
- CCDC28B
- CCDC78
- CCDC88C
- CDH15
- CDK5RAP2
- CDK6
- CDKL5
- CDKN1C
- CDON
- CENPJ
- CEP135
- CEP152
- CEP290
- CEP41
- CEP57
- CEP63
- CERS1
- CHAMP1
- CHD2
- CHD7
- CHD8
- CHKB
- CHMP1A
- CIC
- CLCN4
- CLCNKB
- CLIC2
- CLN3
- CLN5
- CLN6
- CLN8
- CLPB
- CLTC
- CNKSR2
- CNNM2
- CNTN4
- CNTNAP2
- COG1
- COG6
- COG8
- COL4A1
- COL4A3BP
- COQ2
- COX10
- COX14
- COX15
- COX20
- COX6B1
- COX7B
- CPLANE1
- CPLX1
- CPS1
- CRADD
- CRBN
- CREBBP
- CSPP1
- CTBP1
- CTCF
- CTDP1
- CTNNB1
- CTNND2
- CTSA
- CTSD
- CUL3
- CUL4B
- CWF19L1
- CYB5R3
- D2HGDH
- DAG1
- DBT
- DCAF17
- DCHS1
- DCX
- DDHD2
- DDX11
- DDX3X
- DDX59
- DEAF1
- DHCR7
- DIP2C
- DKC1
- DLAT
- DLG3
- DLGAP2
- DMD
- DMPK
- DNAJC19
- DNAJC5
- DNM1
- DNMT3B
- DOCK8
- DPAGT1
- DPM1
- DPP6
- DPYD
- DPYS
- DSCAM
- DYM
- DYNC1H1
- DYRK1A
- EBP
- EDC3
- EEF1A2
- EFTUD2
- EHMT1
- EIF2AK3
- EIF2S3
- EIF4A3
- EIF4E
- ELOVL4
- ELP2
- EPB41L1
- ERBIN
- ERCC2
- ERCC3
- ERCC6
- ERCC8
- ERLIN2
- ESCO2
- ETHE1
- EXOSC3
- EZH2
- FAM126A
- FANCA
- FANCC
- FANCD2
- FANCE
- FAR1
- FASTKD2
- FAT4
- FBN1
- FBXL4
- FBXO31
- FGD1
- FGFR1
- FGFR2
- FGFR3
- FH
- FKRP
- FKTN
- FLNA
- FMN2
- FMR1
- FOLR1
- FOXG1
- FOXP1
- FOXP2
- FOXRED1
- FRAS1
- FRMPD4
- FTSJ1
- FUCA1
- GABRA1
- GABRB3
- GAD1
- GALC
- GALE
- GALT
- GAMT
- GATAD2B
- GATM
- GCH1
- GCK
- GCSH
- GDI1
- GFAP
- GIGYF2
- GJC2
- GK
- GLB1
- GLDC
- GLI3
- GLYCTK
- GMPPA
- GMPPB
- GNAO1
- GNAS
- GNB1
- GNPAT
- GNPTAB
- GNS
- GORAB
- GPC3
- GPHN
- GPT2
- GRIA1
- GRIA3
- GRID2
- GRIK2
- GRIN1
- GRIN2A
- GRIN2B
- GRIP1
- GRN
- GSS
- GTF2H5
- GUSB
- HCCS
- HCFC1
- HCN1
- HDAC4
- HDAC8
- HEPACAM
- HERC2
- HEXA
- HIVEP2
- HLCS
- HMGB3
- HNMT
- HNRNPU
- HOXA1
- HPD
- HPRT1
- HRAS
- HSD17B10
- HSPD1
- HUWE1
- IDS
- IDUA
- IER3IP1
- IGBP1
- IGF1
- IKBKG
- IL1RAPL1
- ILF2
- IMPA1
- INPP5E
- INTS6
- IQSEC2
- IRF2BPL
- ISPD
- ITGA7
- ITPR1
- JAG1
- JMJD1C
- KANK1
- KANSL1
- KAT2B
- KAT6A
- KAT6B
- KATNAL2
- KATNB1
- KCNA2
- KCND2
- KCNH1
- KCNJ1
- KCNJ10
- KCNJ11
- KCNK9
- KCNQ2
- KCNQ5
- KCTD7
- KDM5B
- KDM5C
- KDM6A
- KDM6B
- KIF11
- KIF1A
- KIF1BP
- KIF2A
- KIF4A
- KIF5C
- KIF7
- KIRREL3
- KLHL15
- KMT2A
- KMT2C
- KMT2D
- KMT5B
- KNL1
- KPTN
- KRAS
- L1CAM
- L2HGDH
- LAMA1
- LAMA2
- LAMP2
- LARGE1
- LARP7
- LARS
- LAS1L
- LIAS
- LIG4
- LINS1
- LMAN2L
- LONP1
- LRP2
- LRPPRC
- LYRM7
- MAF
- MAGEL2
- MAN1B1
- MAN2B1
- MANBA
- MAOA
- MAP2K1
- MAP2K2
- MAT1A
- MBD5
- MBOAT7
- MBTPS2
- MCCC1
- MCCC2
- MCOLN1
- MCPH1
- MECP2
- MED12
- MED13
- MED13L
- MED17
- MED23
- MEF2C
- MET
- METTL23
- MFSD8
- MGAT2
- MID1
- MID2
- MIR17HG
- MKKS
- MKS1
- MLYCD
- MMACHC
- MMADHC
- MOCS1
- MOCS2
- MOGS
- MPDU1
- MPDZ
- MPV17
- MRPS22
- MTFMT
- MTHFR
- MTO1
- MTOR
- MTR
- MTRR
- MYCN
- MYO5A
- MYT1L
- NAA10
- NAA15
- NAGA
- NAGLU
- NBN
- NCKAP1
- NDE1
- NDP
- NDST1
- NDUFA1
- NDUFA11
- NDUFA12
- NDUFS1
- NDUFS2
- NDUFS3
- NDUFS4
- NDUFS7
- NDUFS8
- NDUFV1
- NEDD4L
- NEU1
- NEXMIF
- NF1
- NFIA
- NFIX
- NHS
- NIPBL
- NKX2-1
- NLGN3
- NLGN4X
- NONO
- NOP10
- NPC1
- NPC2
- NPHP1
- NR2F1
- NRAS
- NRXN1
- NRXN3
- NSD1
- NSDHL
- NSUN2
- NTNG1
- NTRK1
- NUP62
- NUS1
- OCLN
- OCRL
- OFD1
- OGT
- OPHN1
- ORC1
- OTC
- PACS1
- PAFAH1B1
- PAH
- PAK3
- PANK2
- PAX1
- PC
- PCDH19
- PCNT
- PDE4D
- PDHA1
- PDHX
- PDP1
- PDSS1
- PEPD
- PET100
- PEX1
- PEX10
- PEX11B
- PEX12
- PEX13
- PEX16
- PEX19
- PEX2
- PEX3
- PEX5
- PEX6
- PEX7
- PGAP1
- PGAP2
- PGK1
- PGM3
- PHF3
- PHF6
- PHF8
- PHGDH
- PHIP
- PIGA
- PIGC
- PIGG
- PIGL
- PIGN
- PIGO
- PIGT
- PIGV
- PIGW
- PIK3R2
- PLA2G6
- PLCB1
- PLK4
- PLP1
- PMM2
- PNKP
- PNP
- PNPLA6
- POGZ
- POLG
- POLR3A
- POLR3B
- POMGNT1
- POMK
- POMT1
- POMT2
- PORCN
- POU1F1
- PPM1D
- PPP2R1A
- PPP2R5D
- PPT1
- PQBP1
- PRMT7
- PRODH
- PRPS1
- PRSS12
- PSAP
- PSPH
- PTCH1
- PTCHD1
- PTEN
- PTPN11
- PTRH2
- PTS
- PUF60
- PURA
- PUS1
- PUS3
- PYCR1
- QDPR
- RAB18
- RAB39B
- RAB3GAP1
- RAB3GAP2
- RAC1
- RAD21
- RAF1
- RAI1
- RANBP17
- RANBP2
- RARS2
- RBBP8
- RBM10
- RBM28
- RBMX
- RECQL4
- RELN
- RERE
- RFT1
- RIMS1
- RIT1
- RLIM
- RNASEH2A
- RNASEH2B
- RNASEH2C
- RNASET2
- RNF125
- ROGDI
- ROR2
- RPGRIP1L
- RPL10
- RPS6KA3
- RRM2B
- RTTN
- RUBCN
- RUSC2
- SALL1
- SASS6
- SATB2
- SC5D
- SCAPER
- SCN1A
- SCN2A
- SCN8A
- SCN9A
- SCO1
- SCO2
- SDCCAG8
- SDHA
- SDHAF1
- SEMA3E
- SEMA5A
- SEPSECS
- SERAC1
- SETBP1
- SETD2
- SETD5
- SGSH
- SHANK2
- SHANK3
- SHH
- SHOC2
- SHROOM4
- SIL1
- SIN3A
- SIX3
- SKI
- SLC12A6
- SLC16A2
- SLC17A5
- SLC1A1
- SLC25A15
- SLC2A1
- SLC35A1
- SLC35A3
- SLC35C1
- SLC4A4
- SLC6A1
- SLC6A17
- SLC6A19
- SLC6A3
- SLC6A8
- SLC7A7
- SLC9A6
- SLC9A9
- SMAD4
- SMARCA2
- SMARCA4
- SMARCB1
- SMARCC2
- SMARCE1
- SMC1A
- SMC3
- SMOC1
- SMPD1
- SMS
- SNAP29
- SNIP1
- SNRPN
- SOBP
- SOS1
- SOX10
- SOX11
- SOX2
- SOX3
- SOX5
- SPAST
- SPECC1L
- SPG11
- SPTAN1
- SRCAP
- SRD5A3
- SRPX2
- SRSF11
- SSR4
- ST3GAL3
- ST3GAL5
- STAG1
- STIL
- STRA6
- STT3A
- STT3B
- STXBP1
- SUCLA2
- SUCLG1
- SUMF1
- SUOX
- SURF1
- SYN1
- SYNGAP1
- SYP
- TACO1
- TAF1
- TAF13
- TAF2
- TAF6
- TAOK2
- TAT
- TBC1D20
- TBC1D24
- TBC1D7
- TBCE
- TBL1XR1
- TBR1
- TCF20
- TCF4
- TCN2
- TCTN2
- TCTN3
- TECR
- TFAP2A
- TGFBR2
- THOC2
- THOC6
- TIMM8A
- TMCO1
- TMEM165
- TMEM216
- TMEM231
- TMEM237
- TMEM240
- TMEM67
- TMLHE
- TNIK
- TNRC6B
- TRAPPC9
- TREX1
- TRIM32
- TRIO
- TRIP12
- TRMT10A
- TSC1
- TSC2
- TSEN54
- TSFM
- TSHB
- TSPAN7
- TTC19
- TTC8
- TTI2
- TUBA1A
- TUBA8
- TUBB2B
- TUBB3
- TUBGCP6
- TUSC3
- TWIST1
- TWNK
- UBE2A
- UBE3A
- UBE3B
- UBN2
- UBR1
- UPB1
- UPF3B
- UQCRQ
- UROC1
- USP15
- USP27X
- USP7
- USP9X
- VLDLR
- VPS13B
- VPS37A
- VPS53
- VRK1
- WAC
- WASHC4
- WDFY3
- WDR19
- WDR45
- WDR45B
- WDR62
- WDR73
- WDR81
- WNT5A
- WWOX
- XPA
- XPNPEP3
- XPR1
- XYLT1
- YY1
- ZBTB16
- ZBTB18
- ZBTB20
- ZBTB24
- ZC3H14
- ZC4H2
- ZDHHC15
- ZDHHC9
- ZEB2
- ZFYVE26
- ZIC2
- ZMYND11
- ZNF526
- ZNF592
- ZNF711
- ZSWIM6
EXOMAS
Hipotonías Congénitas
Ref. 4203
33 genes
- CDKL5
- DMPK
- EGR2
- FKRP
- FKTN
- LAMA2
- LARGE1
- MCEE
- MECP2
- MMAA
- MMAB
- MMADHC
- MPZ
- MTM1
- MUT
- PEX1
- PEX10
- PEX12
- PEX13
- PEX14
- PEX16
- PEX19
- PEX2
- PEX26
- PEX3
- PEX5
- PEX6
- PMM2
- PMP22
- POMGNT1
- POMT1
- RYR1
- TAZ
EXOMAS
Artrogriposis Distal
Ref. 3717
10 genes
- ECEL1
- FBN2
- MYBPC1
- MYH3
- MYH8
- PIEZO2
- TNNI2
- TNNT3
- TPM2
- UBA1
EXOMAS
Sobrecrecimiento, Síndromes
Ref. 10077
73 genes
- ABCC9
- AKT1
- APC2
- BMPR1A
- CBS
- CDC45
- CDC6
- CDKN1C
- CDT1
- CHD8
- COL11A1
- COL11A2
- COL2A1
- COL3A1
- COL5A1
- COL5A2
- COL9A1
- COL9A2
- COL9A3
- DICER1
- DIS3L2
- DNMT3A
- EED
- EZH2
- FBN1
- FBN2
- FIBP
- FLCN
- GMNN
- GPC3
- GPC4
- HERC1
- HIST1H1E
- HRAS
- IGF2
- KCNQ1
- KLLN
- MCM5
- MTOR
- MYO5A
- NF1
- NFIX
- NSD1
- OFD1
- ORC1
- ORC4
- ORC6
- PDGFRB
- PIK3CA
- PLOD1
- PPP2R5B
- PPP2R5C
- PPP2R5D
- PTCH1
- PTEN
- RNF125
- RNF135
- SDHB
- SDHC
- SDHD
- SEC23B
- SETD2
- SMAD3
- SMAD4
- STK11
- SUFU
- SUZ12
- TCF20
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
- ZBTB20
EXOMAS
Sobrecrecimiento, Síndromes
Ref. 4674
44 genes
- ABCC9
- AKT1
- APC2
- CDC45
- CDC6
- CDKN1C
- CDT1
- CHD8
- DICER1
- DIS3L2
- DNMT3A
- EED
- EZH2
- FBN1
- FIBP
- GMNN
- GPC3
- GPC4
- HERC1
- HIST1H1E
- IGF2
- KLLN
- MCM5
- MTOR
- MYO5A
- NFIX
- NSD1
- OFD1
- ORC1
- ORC4
- ORC6
- PDGFRB
- PIK3CA
- PPP2R5B
- PPP2R5C
- PPP2R5D
- PTEN
- RNF125
- RNF135
- SEC23B
- SETD2
- SUZ12
- TCF20
- ZBTB20
EXOMAS
Sobrecrecimiento, Síndromes
Ref. 4197
32 genes
- AKT1
- APC2
- CDC45
- CDC6
- CDKN1C
- CDT1
- DICER1
- DIS3L2
- DNMT3A
- EED
- EZH2
- FBN1
- GMNN
- GPC3
- GPC4
- HERC1
- IGF2
- KLLN
- MCM5
- MYO5A
- NFIX
- NSD1
- OFD1
- ORC1
- ORC4
- ORC6
- PIK3CA
- PTEN
- RNF135
- SEC23B
- SETD2
- SUZ12
EXOMAS
Talla baja
Ref. 4684
135 genes
- A2ML1
- ACAN
- AGPS
- ALPL
- ANKRD11
- ARSB
- ARSE
- ATR
- ATRX
- BLM
- BRAF
- BRD4
- BTK
- CBL
- CDC45
- CDC6
- CDT1
- CENPJ
- CEP152
- CEP63
- COL10A1
- COL1A1
- COL1A2
- COL2A1
- COL9A1
- COL9A2
- COL9A3
- COLEC10
- COLEC11
- COMP
- CREBBP
- CRTAP
- CTSK
- CUL7
- DHCR7
- DNA2
- EBP
- EP300
- ERCC3
- ERCC4
- ERCC5
- ERCC6
- ERCC8
- EXT1
- EXT2
- FGD1
- FGF23
- FGFR3
- FLNB
- GALNS
- GH1
- GHR
- GHRHR
- GHSR
- GLB1
- GLI2
- GMNN
- GNAS
- GNPAT
- GUSB
- HDAC8
- HESX1
- HRAS
- HSPG2
- IDS
- IDUA
- IGF1
- IGF1R
- IGFALS
- INSR
- KDM6A
- KMT2D
- KRAS
- LHX3
- LIFR
- LTBP3
- LZTR1
- MAP2K1
- MAP2K2
- MASP1
- MATN3
- MCM5
- MRAS
- NBN
- NF1
- NIN
- NIPBL
- NME1
- NPPC
- NPR2
- NRAS
- NSMCE2
- ORC1
- ORC4
- ORC6
- P3H1
- PACS1
- PEX7
- PHEX
- POU1F1
- PPP1CB
- PROP1
- PTPN11
- RAD21
- RAF1
- RAI1
- RASA2
- RBBP8
- RIT1
- RNPC3
- ROR2
- RPS6KA3
- RRAS
- RRAS2
- RUNX2
- SHOC2
- SHOX
- SLC26A2
- SMARCAL1
- SMC1A
- SMC3
- SOS1
- SOS2
- SOX3
- SPRED1
- STAG1
- STAG2
- STAT5B
- TBCE
- THRB
- TRAIP
- TRAPPC2
- TRIM37
- TRPS1
- WRN
EXOMAS
Lisosomales, Enfermedades
Ref. 3735
48 genes
- AGA
- ARSA
- ARSB
- ASAH1
- CLN3
- CLN5
- CLN6
- CLN8
- CTNS
- CTSA
- CTSD
- CTSK
- FUCA1
- GAA
- GALC
- GALNS
- GBA
- GLA
- GLB1
- GM2A
- GNPTAB
- GNPTG
- GNS
- GUSB
- HEXA
- HEXB
- HGSNAT
- HYAL1
- IDS
- IDUA
- LAMP2
- LIPA
- MAN2B1
- MANBA
- MCOLN1
- MFSD8
- NAGA
- NAGLU
- NEU1
- NPC1
- NPC2
- PPT1
- PSAP
- SGSH
- SLC17A5
- SMPD1
- SUMF1
- TPP1
EXOMAS
Interrupción de Tallo Hipofisiario, Síndrome
Ref. 3737
12 genes
- CDON
- GLI2
- GPR161
- HESX1
- LHX3
- LHX4
- OTX2
- POU1F1
- PROKR2
- PROP1
- SOX3
- TGIF1
EXOMAS
Telangiectasia Hemorrágica Hereditaria
Ref. 3740
5 genes
- ACVRL1
- BMPR2
- ENG
- GDF2
- SMAD4
EXOMAS
Poliquísticos Renales, Síndromes
Ref. 3806
111 genes
- AHI1
- ANKS6
- ARL13B
- ARL3
- ARL6
- ARMC9
- B9D1
- B9D2
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- C8orf37
- CC2D2A
- CCDC28B
- CEP104
- CEP120
- CEP164
- CEP290
- CEP41
- CEP83
- COL4A3
- COL4A4
- COL4A5
- CPLANE1
- CSPP1
- DCDC2
- DYNC2H1
- DYNC2LI1
- EVC
- EVC2
- GLIS2
- HNF1B
- IFT140
- IFT172
- IFT27
- IFT43
- IFT52
- IFT74
- IFT80
- INPP5E
- INVS
- IQCB1
- KIAA0556
- KIAA0586
- KIF14
- KIF7
- LZTFL1
- MAPKBP1
- MET
- MKKS
- MKS1
- MUC1
- NEK1
- NEK8
- NPHP1
- NPHP3
- NPHP4
- OFD1
- PDE6D
- PEX1
- PEX10
- PEX11B
- PEX12
- PEX13
- PEX14
- PEX16
- PEX19
- PEX2
- PEX26
- PEX3
- PEX5
- PEX6
- PEX7
- PKD1
- PKD2
- PKHD1
- RPGRIP1L
- SDCCAG8
- SUFU
- TCTEX1D2
- TCTN1
- TCTN2
- TCTN3
- TMEM107
- TMEM138
- TMEM216
- TMEM231
- TMEM237
- TMEM67
- TRAF3IP1
- TRIM32
- TSC1
- TSC2
- TTC21B
- TTC8
- UMOD
- VHL
- WDPCP
- WDR19
- WDR34
- WDR35
- WDR60
- WT1
- XPNPEP3
- ZNF423
EXOMAS
Poliquísticos Renales, Síndromes
Ref. 4694
93 genes
- AHI1
- ANKS6
- ARL13B
- ARL3
- ARL6
- ARMC9
- B9D1
- B9D2
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- C8orf37
- CC2D2A
- CCDC28B
- CEP104
- CEP120
- CEP164
- CEP290
- CEP41
- CEP83
- CPLANE1
- CSPP1
- DCDC2
- DYNC2H1
- DYNC2LI1
- EVC
- EVC2
- GLIS2
- HNF1B
- IFT140
- IFT172
- IFT27
- IFT43
- IFT52
- IFT74
- IFT80
- INPP5E
- INVS
- IQCB1
- KIAA0556
- KIAA0586
- KIF14
- KIF7
- LZTFL1
- MAPKBP1
- MET
- MKKS
- MKS1
- MUC1
- NEK1
- NEK8
- NPHP1
- NPHP3
- NPHP4
- OFD1
- PDE6D
- PKD1
- PKD2
- PKHD1
- RPGRIP1L
- SDCCAG8
- SUFU
- TCTEX1D2
- TCTN1
- TCTN2
- TCTN3
- TMEM107
- TMEM138
- TMEM216
- TMEM231
- TMEM237
- TMEM67
- TRAF3IP1
- TRIM32
- TSC1
- TSC2
- TTC21B
- TTC8
- UMOD
- VHL
- WDPCP
- WDR19
- WDR34
- WDR35
- WDR60
- XPNPEP3
- ZNF423
EXOMAS
Malformaciones congénitas del riñón y del tracto urinario (CAKUT)
Ref. 4032
37 genes
- ACE
- AGT
- AGTR1
- ANOS1
- BMP4
- CHD1L
- CHRM3
- DSTYK
- EYA1
- FGF20
- FRAS1
- FREM1
- FREM2
- GATA3
- GRIP1
- HNF1B
- HPSE2
- ITGA8
- LRIG2
- MUC1
- NOTCH2
- PAX2
- REN
- RET
- ROBO2
- SALL1
- SIX1
- SIX2
- SIX5
- SOX17
- SRGAP1
- TBX18
- TNXB
- TRAP1
- UMOD
- UPK3A
- WNT4
EXOMAS
Albinismo oculocutáneo
Ref. 3746
7 genes
- LRMDA
- MC1R
- OCA2
- SLC24A5
- SLC45A2
- TYR
- TYRP1
EXOMAS
Atrofia Óptica
Ref. 10060
9 genes
- ACO2
- AFG3L2
- DNM1L
- OPA1
- OPA3
- RTN4IP1
- SSBP1
- TMEM126A
- YME1L1
EXOMAS
Atrofia Óptica
Ref. 4034
7 genes
- ACO2
- DNM1L
- OPA1
- OPA3
- RTN4IP1
- TMEM126A
- YME1L1
EXOMAS
Cataratas congénitas
Ref. 4752
37 genes
- AGK
- BFSP1
- BFSP2
- CHMP4B
- CRYAA
- CRYAB
- CRYBA1
- CRYBA2
- CRYBA4
- CRYBB1
- CRYBB2
- CRYBB3
- CRYGB
- CRYGC
- CRYGD
- CRYGS
- DNMBP
- EPHA2
- FOXE3
- FYCO1
- GCNT2
- GJA3
- GJA8
- HSF4
- LEMD2
- LIM2
- LSS
- MAF
- MIP
- NHS
- PITX3
- SIPA1L3
- SLC16A12
- TDRD7
- UNC45B
- VIM
- WFS1
EXOMAS
Cataratas congénitas
Ref. 3748
35 genes
- AGK
- BFSP1
- BFSP2
- CHMP4B
- CRYAA
- CRYAB
- CRYBA1
- CRYBA2
- CRYBA4
- CRYBB1
- CRYBB2
- CRYBB3
- CRYGB
- CRYGC
- CRYGD
- CRYGS
- EPHA2
- FOXE3
- FYCO1
- GCNT2
- GJA3
- GJA8
- HSF4
- LEMD2
- LIM2
- LSS
- MAF
- MIP
- NHS
- PITX3
- SIPA1L3
- TDRD7
- UNC45B
- VIM
- WFS1
EXOMAS
Hipoacusia Sindrómica
Ref. 4311
141 genes
- ACTG1
- ADCY1
- ADGRV1
- AIFM1
- ATP2B2
- BDP1
- BSND
- BTD
- CABP2
- CCDC50
- CD164
- CDC14A
- CDH23
- CDH7
- CEACAM16
- CIB2
- CLDN14
- CLIC5
- CLRN1
- COCH
- COL11A1
- COL11A2
- COL2A1
- COL4A3
- COL4A4
- COL4A5
- COL4A6
- COL9A1
- COL9A2
- COL9A3
- CRYM
- DCDC2
- DIABLO
- DIAPH1
- DMXL2
- DSPP
- EDN3
- EDNRB
- ELMOD3
- EPS8
- EPS8L2
- ESPN
- ESRP1
- ESRRB
- EYA1
- EYA4
- FAM189A2
- FOXI1
- GAB1
- GIPC3
- GJB2
- GJB3
- GJB6
- GPRASP2
- GPSM2
- GRHL2
- GRXCR1
- GRXCR2
- GSDME
- HARS
- HGF
- HOMER2
- ILDR1
- KARS
- KCNE1
- KCNJ10
- KCNQ1
- KCNQ4
- KITLG
- LHFPL5
- LOXHD1
- LRTOMT
- MARVELD2
- MCM2
- MET
- MITF
- MPZL2
- MSRB3
- MYH14
- MYH9
- MYO15A
- MYO1A
- MYO3A
- MYO6
- MYO7A
- NARS2
- NF2
- NLRP3
- OSBPL2
- OTOA
- OTOF
- OTOG
- OTOGL
- P2RX2
- PAX3
- PCDH15
- PDE1C
- PDZD7
- PEX7
- PHYH
- PJVK
- PNPT1
- POU3F4
- POU4F3
- PPIP5K2
- PRPS1
- RDX
- RIPOR2
- ROR1
- S1PR2
- SEMA3E
- SERPINB6
- SIX1
- SIX5
- SLC17A8
- SLC22A4
- SLC26A4
- SLC26A5
- SLC44A4
- SMPX
- SOX10
- STRC
- SYNE4
- TBC1D24
- TECTA
- TIMM8A
- TJP2
- TMC1
- TMEM132E
- TMIE
- TMPRSS3
- TNC
- TPRN
- TRIOBP
- TSPEAR
- USH1C
- USH1G
- USH2A
- WBP2
- WFS1
- WHRN
EXOMAS
MAC. Espectro Microftalmia, Anoftalmia, Coloboma.
Ref. 10064
29 genes
- ABCB6
- BCOR
- BMP4
- CHD7
- CRYBA4
- FOXE3
- GDF3
- GDF6
- HCCS
- HESX1
- HMGB3
- MAB21L2
- NAA10
- NHS
- OTX2
- PAX6
- PORCN
- PXDN
- RARB
- RAX
- RBP4
- SHH
- SMOC1
- SOX2
- STRA6
- TENM3
- TFAP2A
- VAX1
- VSX2
EXOMAS
Tubulopatía Renal
Ref. 4093
48 genes
- AQP2
- ATP6V0A4
- ATP6V1B1
- AVPR2
- BSND
- CA2
- CASR
- CLCN5
- CLCNKA
- CLCNKB
- CLDN16
- CLDN19
- CNNM2
- CTNS
- CUL3
- DMP1
- EGF
- ENPP1
- FGF23
- FXYD2
- HNF1B
- KCNA1
- KCNJ1
- KCNJ10
- KLHL3
- MUC1
- OCRL
- PHEX
- REN
- SCNN1A
- SCNN1B
- SCNN1G
- SLC12A1
- SLC12A3
- SLC1A1
- SLC22A12
- SLC2A2
- SLC2A9
- SLC34A1
- SLC34A3
- SLC4A1
- SLC4A4
- SLC5A2
- SLC7A7
- TRPM6
- UMOD
- WNK1
- WNK4
EXOMAS
Diabetes Monogénica
Ref. 3763
37 genes
- ABCC8
- AKT2
- ALMS1
- APPL1
- BLK
- CEL
- CISD2
- CP
- DCAF17
- EIF2AK3
- FOXP3
- GATA6
- GCK
- GLIS3
- GLUD1
- HADH
- HNF1A
- HNF1B
- HNF4A
- IER3IP1
- INS
- INSR
- KCNJ11
- KLF11
- NEUROD1
- NEUROG3
- PAX4
- PAX6
- PDX1
- PTF1A
- RFX6
- SLC19A2
- SLC29A3
- SLC2A2
- TBC1D4
- WFS1
- ZFP57
EXOMAS
Glucogenosis
Ref. 3766
22 genes
- AGL
- ALDOA
- ENO3
- G6PC
- GAA
- GBE1
- GYG1
- GYS1
- GYS2
- LAMP2
- LDHA
- PFKM
- PGAM2
- PGM1
- PHKA1
- PHKA2
- PHKB
- PHKG2
- PRKAG2
- PYGL
- PYGM
- SLC37A4
EXOMAS
Hiperinsulinemia Hipoglucemia
Ref. 3767
9 genes
- ABCC8
- GCK
- GLUD1
- HADH
- HNF4A
- INSR
- KCNJ11
- SLC16A1
- UCP2
EXOMAS
Hiperlaxitud
Ref. 4318
77 genes
- ADAMTS2
- ALDH18A1
- ATP6V0A2
- ATP6V1A
- ATP6V1E1
- ATP7A
- B3GALT6
- B4GALT7
- BMP1
- BRAF
- CANT1
- CBS
- CHST14
- COL11A1
- COL11A2
- COL12A1
- COL1A1
- COL1A2
- COL2A1
- COL3A1
- COL5A1
- COL5A2
- COL6A1
- COL6A2
- COL6A3
- COL9A1
- COL9A2
- COL9A3
- DSE
- EFEMP2
- ELN
- EXOC6B
- FBLN5
- FBN1
- FGD1
- FGFR3
- FKBP10
- FKBP14
- FLNB
- FMR1
- GALNS
- HRAS
- IFITM5
- KDM6A
- KIF22
- KMT2D
- KRAS
- LTBP4
- LZTR1
- MAP2K1
- MAP2K2
- MYH7
- NOTCH3
- NRAS
- PLOD1
- PRDM5
- PTPN11
- PYCR1
- RAF1
- RIT1
- RYR1
- SERPINH1
- SKI
- SLC2A10
- SLC39A13
- SMAD3
- SOS1
- SOS2
- SP7
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
- TNXB
- TTN
- XYLT1
- ZNF469
EXOMAS
Hiperlaxitud
Ref. 3768
81 genes
- ALDH18A1
- ATP6V0A2
- ATP6V1A
- ATP6V1E1
- ATP7A
- B3GALT6
- B4GALT7
- BMP1
- BRAF
- CANT1
- CBS
- CHST14
- COL11A1
- COL11A2
- COL12A1
- COL1A1
- COL1A2
- COL2A1
- COL3A1
- COL5A1
- COL5A2
- COL6A1
- COL6A2
- COL6A3
- COL9A1
- COL9A2
- COL9A3
- CST3
- DSE
- EFEMP2
- ELN
- FBLN5
- FBN1
- FGD1
- FGFR3
- FKBP10
- FKBP14
- FLNB
- FMR1
- GALNS
- HRAS
- IFITM5
- IMPAD1
- KDM6A
- KIF22
- KMT2D
- KRAS
- LTBP4
- LZTR1
- MAP2K1
- MAP2K2
- MYH7
- NOTCH3
- NRAS
- PLOD1
- PRDM5
- PTPN11
- PYCR1
- RAF1
- RIT1
- RYR1
- SERPINH1
- SKI
- SLC26A2
- SLC2A10
- SLC39A13
- SMAD3
- SOS1
- SOS2
- SP7
- SSPN
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
- TNXB
- TRPS1
- TTN
- TYMP
- XYLT1
- ZNF469
EXOMAS
Esclerosis Lateral Amiotrófica y/o Demencia Frontotemporal
Ref. 4304
30 genes
- ALS2
- ANG
- ANXA11
- ATXN2
- C9orf72
- CHCHD10
- CHMP2B
- DCTN1
- ERBB4
- FIG4
- FUS
- HNRNPA1
- KIF5A
- MATR3
- NEFH
- NEK1
- OPTN
- PFN1
- PRPH
- SETX
- SIGMAR1
- SOD1
- SPG11
- SQSTM1
- TARDBP
- TBK1
- TUBA4A
- UBQLN2
- VAPB
- VCP
EXOMAS
Esclerosis Lateral Amiotrófica y/o Demencia Frontotemporal
Ref. 3774
29 genes
- ALS2
- ANG
- ANXA11
- ATXN2
- C9orf72
- CHCHD10
- CHMP2B
- DCTN1
- ERBB4
- FIG4
- FUS
- HNRNPA1
- MATR3
- NEFH
- NEK1
- OPTN
- PFN1
- PRPH
- SETX
- SIGMAR1
- SOD1
- SPG11
- SQSTM1
- TARDBP
- TBK1
- TUBA4A
- UBQLN2
- VAPB
- VCP
EXOMAS
Artrogriposis Distal Sindrómica
Ref. 3795
32 genes
- ADCY6
- ADGRG6
- ASCC1
- CHST14
- CNTNAP1
- DNM2
- DOK7
- ECEL1
- ERBB3
- FBN2
- GLDN
- GLE1
- KIF14
- LGI4
- MUSK
- MYBPC1
- MYH3
- MYH8
- NEK9
- PI4KA
- PIEZO2
- RAPSN
- SLC35A3
- TNNI2
- TNNT3
- TPM2
- TRIP4
- UBA1
- VIPAS39
- VPS33B
- ZBTB42
- ZC4H2
EXOMAS
Síndrome de depleción del ADN mitocondrial
Ref. 4583
17 genes
- AGK
- DGUOK
- FBXL4
- MGME1
- MPV17
- MRM2
- OPA1
- POLG
- POLG2
- RRM2B
- SLC25A4
- SUCLA2
- SUCLG1
- TFAM
- TK2
- TWNK
- TYMP
EXOMAS
Síndrome de depleción del ADN mitocondrial
Ref. 4584
17 genes
- AGK
- DGUOK
- FBXL4
- MGME1
- MPV17
- MRM2
- OPA1
- POLG
- POLG2
- RRM2B
- SLC25A4
- SUCLA2
- SUCLG1
- TFAM
- TK2
- TWNK
- TYMP
EXOMAS
Arritmias
Ref. 4284
93 genes
- ABCC9
- ACTC1
- ACTN2
- AKAP9
- ALG10B
- ANK2
- ANKRD1
- BAG3
- CACNA1C
- CACNA2D1
- CACNB2
- CALM1
- CALM2
- CASQ2
- CAV3
- CRYAB
- CSRP3
- CTNNA3
- DES
- DMD
- DSC2
- DSG2
- DSP
- EMD
- EYA4
- FGF12
- FHL1
- FHL2
- FKRP
- FKTN
- GATAD1
- GPD1L
- HCN4
- HFE
- ILK
- JUP
- KCND2
- KCND3
- KCNE1
- KCNE2
- KCNE3
- KCNE5
- KCNH2
- KCNJ2
- KCNJ5
- KCNJ8
- KCNQ1
- LAMA4
- LAMP2
- LDB3
- LMNA
- MYBPC3
- MYH6
- MYH7
- MYPN
- NEXN
- PDLIM3
- PKP2
- PLN
- PRDM16
- PSEN1
- PSEN2
- RAF1
- RANGRF
- RBM20
- RYR2
- SCN10A
- SCN1B
- SCN2B
- SCN3B
- SCN4B
- SCN5A
- SDHA
- SEMA3A
- SGCD
- SLMAP
- SNTA1
- TAZ
- TBX20
- TCAP
- TECRL
- TGFB3
- TMEM43
- TMPO
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TRDN
- TRPM4
- TTN
- TXNRD2
- VCL
EXOMAS
Canalopatías
Ref. 3861
80 genes
- ABCC8
- ABCC9
- ATP1A2
- BEST1
- BSND
- CACNA1A
- CACNA1C
- CACNA1F
- CACNA1H
- CACNA1S
- CACNA2D1
- CACNB2
- CACNB4
- CHRNA1
- CHRNA2
- CHRNA4
- CHRNB1
- CHRNB2
- CHRND
- CHRNE
- CHRNG
- CLCN1
- CLCN2
- CLCN7
- CLCNKA
- CLCNKB
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- GABRA1
- GABRA6
- GABRB3
- GABRD
- GABRG2
- GLRA1
- GLRB
- HCN4
- KCNA1
- KCNA5
- KCNC3
- KCNE1
- KCNE2
- KCNE3
- KCNH2
- KCNJ1
- KCNJ10
- KCNJ11
- KCNJ2
- KCNJ5
- KCNMA1
- KCNQ1
- KCNQ2
- KCNQ3
- KCNQ4
- KCNT1
- MCOLN1
- OSTM1
- PKD2
- RYR1
- RYR2
- SCN1A
- SCN1B
- SCN2A
- SCN3B
- SCN4A
- SCN4B
- SCN5A
- SCN8A
- SCN9A
- SCNN1A
- SCNN1B
- SCNN1G
- SLC1A3
- TRPA1
- TRPC6
- TRPM1
- TRPM4
- TRPM6
- TRPV4
EXOMAS
Canalopatías del Sistema Nervioso
Ref. 3862
49 genes
- ATP1A2
- BEST1
- CACNA1A
- CACNA1F
- CACNA1H
- CACNA1S
- CACNB4
- CHRNA1
- CHRNA2
- CHRNA4
- CHRNB1
- CHRNB2
- CHRND
- CHRNE
- CHRNG
- CLCN1
- CLCN2
- CNGA1
- CNGA3
- CNGB1
- CNGB3
- GABRA1
- GABRA6
- GABRB3
- GABRD
- GABRG2
- GLRA1
- GLRB
- KCNA1
- KCNC3
- KCNJ10
- KCNJ2
- KCNMA1
- KCNQ2
- KCNQ3
- KCNQ4
- KCNT1
- MCOLN1
- RYR1
- SCN1A
- SCN1B
- SCN2A
- SCN4A
- SCN8A
- SCN9A
- SLC1A3
- TRPA1
- TRPM1
- TRPV4
EXOMAS
Canalopatías Cardiacas
Ref. 3863
19 genes
- ABCC9
- CACNA1C
- CACNA2D1
- CACNB2
- HCN4
- KCNA5
- KCNE1
- KCNE2
- KCNE3
- KCNH2
- KCNJ2
- KCNJ5
- KCNQ1
- RYR2
- SCN1B
- SCN3B
- SCN4B
- SCN5A
- TRPM4
EXOMAS
Canalopatías Endocrinas
Ref. 3864
5 genes
- ABCC8
- CLCN7
- KCNJ11
- KCNJ5
- OSTM1
EXOMAS
Canalopatías Renales
Ref. 3865
10 genes
- BSND
- CLCNKA
- CLCNKB
- KCNJ1
- PKD2
- SCNN1A
- SCNN1B
- SCNN1G
- TRPC6
- TRPM6
EXOMAS
Cáncer hereditario
Ref. 3887
50 genes
- ABRAXAS1
- APC
- ATM
- BARD1
- BMPR1A
- BRCA1
- BRCA2
- BRIP1
- CDH1
- CDK4
- CDKN2A
- CHEK2
- EPCAM
- FH
- KIF1B
- MAX
- MEN1
- MET
- MLH1
- MLH3
- MRE11
- MSH2
- MSH3
- MSH6
- MUTYH
- NBN
- NF1
- NTHL1
- PALB2
- PIK3CA
- PMS2
- POLD1
- POLE
- PTEN
- RAD50
- RAD51C
- RAD51D
- RB1
- RET
- SDHA
- SDHAF2
- SDHB
- SDHC
- SDHD
- SMAD4
- STK11
- TMEM127
- TP53
- VHL
- XRCC2
EXOMAS
Cáncer de mama hereditario
Ref. 3888
18 genes
- ATM
- BARD1
- BRCA1
- BRCA2
- BRIP1
- CDH1
- CHEK2
- MRE11
- NBN
- NF1
- PALB2
- PTEN
- RAD50
- RAD51C
- RAD51D
- STK11
- TP53
- XRCC2
EXOMAS
Cáncer de mama hereditario
Ref. 10061
2 genes
- BRCA1
- BRCA2
EXOMAS
Cáncer de ovario hereditario
Ref. 3889
11 genes
- BRCA1
- BRCA2
- BRIP1
- EPCAM
- MLH1
- MSH2
- MSH6
- PMS2
- RAD51C
- RAD51D
- STK11
EXOMAS
Cáncer de mama y ovario hereditario
Ref. 3890
23 genes
- ATM
- BARD1
- BRCA1
- BRCA2
- BRIP1
- CDH1
- CHEK2
- EPCAM
- MLH1
- MRE11
- MSH2
- MSH6
- NBN
- NF1
- PALB2
- PMS2
- PTEN
- RAD50
- RAD51C
- RAD51D
- STK11
- TP53
- XRCC2
EXOMAS
Cáncer de útero hereditario
Ref. 3891
5 genes
- EPCAM
- MLH1
- MSH2
- MSH6
- PTEN
EXOMAS
Cáncer colorrectal hereditario
Ref. 3892
18 genes
- APC
- ATM
- BMPR1A
- CHEK2
- EPCAM
- MLH1
- MSH2
- MSH3
- MSH6
- MUTYH
- NTHL1
- PMS2
- POLD1
- POLE
- PTEN
- SMAD4
- STK11
- TP53
EXOMAS
Cáncer pancreático hereditario
Ref. 3895
8 genes
- BRCA1
- BRCA2
- CDKN2A
- MLH1
- MSH2
- MSH6
- SMAD4
- STK11
EXOMAS
Mucopolisacaridosis
Ref. 3904
11 genes
- ARSB
- GALNS
- GLB1
- GNS
- GUSB
- HGSNAT
- HYAL1
- IDS
- IDUA
- NAGLU
- SGSH
EXOMAS
Miopatías Metabólicas
Ref. 3924
39 genes
- ABHD5
- ACADL
- ACADM
- ACADS
- ACADVL
- AGL
- ALDOA
- CACNA1S
- CLCN1
- CPT1A
- CPT2
- ENO3
- ETFA
- ETFB
- ETFDH
- GAA
- GBE1
- GYG1
- GYS1
- HADHA
- HADHB
- KCNA1
- KCNE3
- LDHA
- LPIN1
- MICU1
- MTO1
- PFKM
- PGAM2
- PGK1
- PGM1
- PHKA1
- PNPLA2
- PRKAG2
- PYGM
- SCN4A
- SLC22A5
- SLC25A20
- TAZ
EXOMAS
Polidactilia
Ref. 3932
33 genes
- ARL6
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- CCDC28B
- CEP290
- DHCR7
- DYNC2H1
- EVC
- FGFR2
- GLI3
- IFT27
- LMBR1
- LZTFL1
- MIPOL1
- MKKS
- MKS1
- PITX1
- RAB23
- SDCCAG8
- SHH
- TMEM67
- TRIM32
- TTC8
- TWIST1
- WDPCP
- ZNF141
EXOMAS
Sindactilia
Ref. 3933
36 genes
- ARL6
- BBIP1
- BBS1
- BBS10
- BBS12
- BBS2
- BBS4
- BBS5
- BBS7
- BBS9
- CCDC28B
- CEP290
- DHCR7
- FBLN1
- FGF16
- FGFR1
- FGFR2
- FMN1
- GJA1
- GLI3
- GREM1
- HOXD13
- IFT27
- LMBR1
- LRP4
- LZTFL1
- MKKS
- MKS1
- RAB23
- SDCCAG8
- SHH
- TMEM67
- TRIM32
- TTC8
- TWIST1
- WDPCP
EXOMAS
Colagenopatías
Ref. 3963
22 genes
- COL10A1
- COL11A1
- COL11A2
- COL17A1
- COL18A1
- COL1A1
- COL1A2
- COL2A1
- COL3A1
- COL4A1
- COL4A2
- COL4A3
- COL4A4
- COL4A5
- COL4A6
- COL5A1
- COL5A2
- COL6A1
- COL7A1
- COL9A1
- COL9A2
- COL9A3
EXOMAS
BAFopatías
Ref. 4764
14 genes
- ADNP
- ARID1A
- ARID1B
- ARID2
- DPF2
- PHF6
- SMARCA2
- SMARCA4
- SMARCB1
- SMARCC2
- SMARCD1
- SMARCE1
- SOX11
- SOX4
EXOMAS
Miopatías
Ref. 3965
108 genes
- ABHD5
- ACADL
- ACADM
- ACADS
- ACADVL
- ACTA1
- AGL
- AGRN
- ALDOA
- ALG14
- ALG2
- ANO5
- BAG3
- BIN1
- CACNA1S
- CCDC7
- CCDC78
- CFL2
- CHAT
- CHRNA1
- CHRNB1
- CHRND
- CHRNE
- CHRNG
- CLCN1
- CNTN1
- COL13A1
- COLQ
- CPT1A
- CPT2
- CRYAB
- DES
- DNM2
- DOK7
- DPAGT1
- DYSF
- ENO3
- ETFA
- ETFB
- ETFDH
- FLNC
- GAA
- GBE1
- GFPT1
- GNE
- GYG1
- GYS1
- HACD1
- HADHA
- HADHB
- HSPG2
- KBTBD13
- KCNA1
- KCNE3
- KLHL40
- KLHL41
- KY
- LAMB2
- LDB3
- LDHA
- LMOD3
- LPIN1
- LRP4
- MAP3K20
- MEGF10
- MICU1
- MMD2
- MTM1
- MTMR14
- MTO1
- MUSK
- MYBPC3
- MYF6
- MYH7
- MYO18B
- MYOT
- MYPN
- NEB
- PFKM
- PGAM2
- PGK1
- PGM1
- PHKA1
- PLEC
- PNPLA2
- PREPL
- PRKAG2
- PYGM
- PYROXD1
- RAPSN
- RYR1
- SCN4A
- SELENON
- SLC18A3
- SLC22A5
- SLC25A20
- SLC5A7
- SNAP25
- SPEG
- STAC3
- STIM1
- SYT2
- TAZ
- TIA1
- TNNT1
- TPM2
- TPM3
- TTN
EXOMAS
Condrodisplasia punctata
Ref. 10082
26 genes
- AGPS
- ARSE
- DHCR24
- DHCR7
- EBP
- GNPAT
- LBR
- MGP
- MSMO1
- NSDHL
- PEX1
- PEX10
- PEX11B
- PEX12
- PEX13
- PEX14
- PEX16
- PEX19
- PEX2
- PEX26
- PEX3
- PEX5
- PEX6
- PEX7
- POR
- SC5D
EXOMAS
Condrodisplasia punctata
Ref. 3990
5 genes
- AGPS
- ARSE
- EBP
- GNPAT
- PEX7
EXOMAS
Displasia frontonasal
Ref. 3999
3 genes
- ALX1
- ALX3
- ALX4
EXOMAS
Epidermólisis bullosa
Ref. 4763
20 genes
- CD151
- COL17A1
- COL7A1
- DSP
- DST
- EXPH5
- FERMT1
- ITGA3
- ITGA6
- ITGB4
- JUP
- KLHL24
- KRT14
- KRT5
- LAMA3
- LAMB3
- LAMC2
- PKP1
- PLEC
- TGM5
EXOMAS
Griscelli, síndrome
Ref. 4005
3 genes
- MLPH
- MYO5A
- RAB27A
EXOMAS
Osteopetrosis
Ref. 4009
9 genes
- CA2
- CLCN7
- LRP5
- OSTM1
- PLEKHM1
- SNX10
- TCIRG1
- TNFRSF11A
- TNFSF11
EXOMAS
Pseudohipoaldosteronismo
Ref. 4010
7 genes
- CUL3
- KLHL3
- SCNN1A
- SCNN1B
- SCNN1G
- WNK1
- WNK4
EXOMAS
Vitreorretinopatía exudativa
Ref. 4012
6 genes
- CTNNB1
- FZD4
- LRP5
- NDP
- TSPAN12
- ZNF408
EXOMAS
Trastornos de la biogénesis del peroxisoma
Ref. 4013
14 genes
- PEX1
- PEX10
- PEX11B
- PEX12
- PEX13
- PEX14
- PEX16
- PEX19
- PEX2
- PEX26
- PEX3
- PEX5
- PEX6
- PEX7
EXOMAS
Panel SNPs Woman
Ref. 4019
EXOMAS
Panel SNPs Age
Ref. 4021
EXOMAS
Panel SNPs Neuroprogram
Ref. 4022
EXOMAS
Ataxia
Ref. 4087
29 genes
- AFG3L2
- ANO10
- APTX
- BEAN1
- CACNA1A
- CACNB4
- COQ8A
- FGF14
- FXN
- IFRD1
- ITPR1
- KCNC3
- MTPAP
- MTTP
- PDYN
- PIK3R5
- PLEKHG4
- PRKCG
- SACS
- SETX
- SLC1A3
- SPTBN2
- SYNE1
- SYT14
- TDP1
- TGM6
- TTBK2
- TTPA
- ZNF592
EXOMAS
Ataxia
Ref. 4312
178 genes
- AAAS
- ABCB7
- ABHD12
- ACO2
- AFG3L2
- AHI1
- ANO10
- APTX
- ARL13B
- ARL3
- ARMC9
- ATCAY
- ATG5
- ATM
- ATN1
- ATP1A3
- ATP2B3
- ATP8A2
- B9D1
- B9D2
- BEAN1
- C9orf72
- CA8
- CACNA1A
- CACNA1G
- CACNB4
- CAPN1
- CASK
- CC2D2A
- CCDC88C
- CEP104
- CEP120
- CEP290
- CEP41
- CHP1
- CLCN2
- CLN5
- CLN6
- COQ8A
- COX20
- CP
- CPLANE1
- CSPP1
- CWF19L1
- CYP27A1
- CYP7B1
- DAB1
- DARS2
- DNAJC19
- DNAJC3
- DNMT1
- EEF2
- EIF2B1
- EIF2B2
- EIF2B3
- EIF2B4
- EIF2B5
- ELOVL4
- ELOVL5
- FAT2
- FGF12
- FGF14
- FLVCR1
- FMR1
- FXN
- GBA2
- GDAP2
- GOSR2
- GRID2
- GRM1
- HEXA
- HEXB
- INPP5E
- ITPR1
- KCNA1
- KCNC3
- KCND3
- KCNJ10
- KIAA0556
- KIAA0586
- KIF1C
- KIF7
- L2HGDH
- LAMA1
- MARS2
- MKS1
- MME
- MRE11
- MTCL1
- MTPAP
- MTTP
- NKX6-2
- NOP56
- NPC1
- NPC2
- NPHP1
- OFD1
- OPA1
- OPHN1
- PCDH12
- PCNA
- PDE6D
- PDYN
- PEX7
- PHYH
- PIBF1
- PIK3R5
- PLA2G6
- PLD3
- PMM2
- PMPCA
- PNKP
- PNPLA6
- POLG
- POLR3A
- POLR3B
- PPP2R2B
- PRKCG
- PTF1A
- PUM1
- RFC1
- RNF216
- RPGRIP1L
- RUBCN
- SACS
- SCN2A
- SCYL1
- SETX
- SIL1
- SLC17A5
- SLC1A3
- SLC25A46
- SLC52A2
- SLC6A19
- SLC9A1
- SLC9A6
- SNX14
- SPG11
- SPG7
- SPTBN2
- SQSTM1
- STUB1
- SUFU
- SYNE1
- SYT14
- TBP
- TCTN1
- TCTN2
- TCTN3
- TDP1
- TDP2
- TGM6
- THG1L
- TMEM107
- TMEM138
- TMEM216
- TMEM231
- TMEM237
- TMEM240
- TMEM67
- TPP1
- TRPC3
- TSFM
- TTBK2
- TTPA
- TUBB4A
- TWNK
- TXN2
- UBA5
- VAMP1
- VLDLR
- VPS13D
- VWA3B
- WDR73
- WDR81
- WFS1
- WWOX
- ZNF423
EXOMAS
Porfiria
Ref. 10052
10 genes
- ALAD
- ALAS2
- CLPX
- CPOX
- FECH
- HFE
- HMBS
- PPOX
- UROD
- UROS
EXOMAS
Braquidactilia
Ref. 4194
11 genes
- BMP2
- BMPR1B
- GDF5
- HDAC4
- HOXD13
- IHH
- NOG
- PDE3A
- PITX1
- PTHLH
- ROR2
EXOMAS
Cáncer pediátrico
Ref. 4231
EXOMAS
Agenesia del cuerpo calloso
Ref. 4289
106 genes
- AHI1
- AMPD2
- ANOS1
- ARID1B
- ARL13B
- ARX
- ASPM
- ATR
- ATRX
- B9D1
- B9D2
- BCOR
- BMP4
- C12orf57
- CASK
- CC2D2A
- CENPJ
- CEP152
- CEP290
- CEP41
- CEP63
- CREBBP
- CTBP1
- DCX
- DHCR24
- DHCR7
- DIS3L2
- DISC1
- EFNB1
- EP300
- EPG5
- FGF8
- FGFR1
- FGFR2
- FH
- FKRP
- FKTN
- FLNA
- GLI3
- GNRH1
- GNRHR
- GPSM2
- HCCS
- HESX1
- HS6ST1
- HYLS1
- IGBP1
- IGF1
- INPP5E
- ISPD
- KAT6B
- KIF7
- KISS1
- KISS1R
- L1CAM
- LARGE1
- LRP2
- MED12
- MID1
- MKS1
- NDE1
- NFIX
- NIN
- NPHP1
- NPHP3
- NSD1
- NSMF
- OFD1
- OTX2
- PAX6
- PDHA1
- PDHB
- POMGNT1
- POMGNT2
- POMT1
- POMT2
- PYCR1
- RAB18
- RAB3GAP1
- RAB3GAP2
- RBBP8
- RBM10
- RELN
- RPGRIP1L
- SEMA3A
- SLC12A6
- SOX2
- SPG11
- STRA6
- TAC3
- TACR3
- TCF4
- TCTN1
- TCTN2
- TCTN3
- TMEM138
- TMEM216
- TMEM237
- TMEM67
- TUBA1A
- TUBB2B
- TUBB3
- VAX1
- WDR11
- WDR62
- ZEB2
EXOMAS
Disgenesia Gonadal (46,XX)
Ref. 4716
9 genes
- BMP15
- ESR2
- FSHR
- MCM9
- MRPS22
- NUP107
- PSMC3IP
- SOHLH1
- SPIDR
EXOMAS
Disgenesia Gonadal (46,XX)
Ref. 4310
8 genes
- BMP15
- ESR2
- FSHR
- MCM9
- MRPS22
- NUP107
- PSMC3IP
- SOHLH1
EXOMAS
Hiperparatiroidismo
Ref. 4354
8 genes
- AP2S1
- CASR
- CDC73
- GCM2
- GNA11
- MEN1
- RET
- TRPV6
EXOMAS
Dislipemia
Ref. 4355
8 genes
- APOA5
- APOB
- LDLR
- LDLRAP1
- LIPI
- LPL
- PCSK9
- USF1
EXOMAS
Cardiopatía estructural
Ref. 4359
90 genes
- ABCC9
- ACTC1
- ACTN2
- ALPK3
- ANKRD1
- BAG3
- BRAF
- CALR3
- CAV3
- CRYAB
- CSRP3
- CTNNA3
- DES
- DMD
- DSC2
- DSG2
- DSP
- DTNA
- EMD
- EYA4
- FHL1
- FHL2
- FKRP
- FKTN
- FLNC
- FXN
- GAA
- GATAD1
- GLA
- HFE
- HRAS
- ILK
- JPH2
- JUP
- KLF10
- KRAS
- LAMA4
- LAMP2
- LDB3
- LMNA
- LZTR1
- MAP2K1
- MAP2K2
- MIB1
- MYBPC3
- MYH6
- MYH7
- MYL2
- MYL3
- MYLK2
- MYOM1
- MYOZ2
- MYPN
- NEXN
- NRAS
- OBSCN
- PDLIM3
- PKP2
- PLN
- PRDM16
- PRKAG2
- PSEN1
- PSEN2
- PTPN11
- RAF1
- RASA2
- RBM20
- RIT1
- RRAS
- RYR2
- SCN5A
- SDHA
- SGCD
- SOS1
- SOS2
- TAZ
- TBX20
- TCAP
- TGFB3
- TMEM43
- TMPO
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TRIM63
- TTN
- TTR
- TXNRD2
- VCL
EXOMAS
Neutropenia
Ref. 4360
17 genes
- AP3B1
- CSF3R
- CXCR4
- DNM2
- ELANE
- G6PC3
- GFI1
- HAX1
- IRAK4
- JAGN1
- SBDS
- SLC37A4
- TAZ
- USB1
- VPS13B
- VPS45
- WAS
EXOMAS
Miocardiopatías
Ref. 10054
165 genes
- ABCC9
- ACTA2
- ACTC1
- ACTN2
- AKAP9
- ALG10B
- ALPK3
- ANK2
- ANKRD1
- B3GAT3
- BAG3
- BRAF
- CACNA1C
- CACNA2D1
- CACNB2
- CALM1
- CALM2
- CALM3
- CALR3
- CASQ2
- CAV3
- CDH2
- COL1A1
- COL1A2
- COL3A1
- COL4A5
- COL5A1
- COL5A2
- CRYAB
- CSRP3
- CTNNA3
- DES
- DMD
- DSC2
- DSG2
- DSP
- DTNA
- EFEMP2
- ELN
- EMD
- EYA4
- FBN1
- FBN2
- FGF12
- FHL1
- FHL2
- FKRP
- FKTN
- FLNA
- FLNC
- FOXE3
- FXN
- GAA
- GATA5
- GATAD1
- GJA5
- GLA
- GPD1L
- HCN4
- HFE
- HRAS
- ILK
- JPH2
- JUP
- KCNA5
- KCND2
- KCND3
- KCNE1
- KCNE2
- KCNE3
- KCNE5
- KCNH2
- KCNJ2
- KCNJ5
- KCNJ8
- KCNQ1
- KLF10
- KRAS
- LAMA4
- LAMP2
- LDB3
- LMNA
- LOX
- LZTR1
- MAP2K1
- MAP2K2
- MAT2A
- MED12
- MFAP5
- MIB1
- MYBPC3
- MYH11
- MYH6
- MYH7
- MYL2
- MYL3
- MYL4
- MYLK
- MYLK2
- MYOM1
- MYOZ2
- MYPN
- NEXN
- NKX2-5
- NOTCH1
- NPPA
- NRAS
- NUP155
- OBSCN
- PDLIM3
- PKP2
- PLN
- PLOD1
- PRDM16
- PRKAG2
- PRKG1
- PSEN1
- PSEN2
- PTPN11
- RAF1
- RANGRF
- RASA2
- RBM20
- RIT1
- RRAS
- RYR2
- SCN10A
- SCN1B
- SCN2B
- SCN3B
- SCN4B
- SCN5A
- SDHA
- SEMA3A
- SGCD
- SKI
- SLC2A10
- SLMAP
- SMAD3
- SMAD4
- SNTA1
- SOS1
- SOS2
- TAZ
- TBX20
- TCAP
- TECRL
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
- TMEM43
- TMPO
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TRDN
- TRIM63
- TRPM4
- TTN
- TTR
- TXNRD2
- VCL
- ZDHHC9
EXOMAS
Miocardiopatías
Ref. 4365
163 genes
- ABCC9
- ACTA2
- ACTC1
- ACTN2
- AKAP9
- ALG10B
- ALPK3
- ANK2
- ANKRD1
- B3GAT3
- BAG3
- BRAF
- CACNA1C
- CACNA2D1
- CACNB2
- CALM1
- CALM2
- CALR3
- CASQ2
- CAV3
- COL1A1
- COL1A2
- COL3A1
- COL4A5
- COL5A1
- COL5A2
- CRYAB
- CSRP3
- CTNNA3
- DES
- DMD
- DSC2
- DSG2
- DSP
- DTNA
- EFEMP2
- ELN
- EMD
- EYA4
- FBN1
- FBN2
- FGF12
- FHL1
- FHL2
- FKRP
- FKTN
- FLNA
- FLNC
- FOXE3
- FXN
- GAA
- GATA5
- GATAD1
- GJA5
- GLA
- GPD1L
- HCN4
- HFE
- HRAS
- ILK
- JPH2
- JUP
- KCNA5
- KCND2
- KCND3
- KCNE1
- KCNE2
- KCNE3
- KCNE5
- KCNH2
- KCNJ2
- KCNJ5
- KCNJ8
- KCNQ1
- KLF10
- KRAS
- LAMA4
- LAMP2
- LDB3
- LMNA
- LOX
- LZTR1
- MAP2K1
- MAP2K2
- MAT2A
- MED12
- MFAP5
- MIB1
- MYBPC3
- MYH11
- MYH6
- MYH7
- MYL2
- MYL3
- MYL4
- MYLK
- MYLK2
- MYOM1
- MYOZ2
- MYPN
- NEXN
- NKX2-5
- NOTCH1
- NPPA
- NRAS
- NUP155
- OBSCN
- PDLIM3
- PKP2
- PLN
- PLOD1
- PRDM16
- PRKAG2
- PRKG1
- PSEN1
- PSEN2
- PTPN11
- RAF1
- RANGRF
- RASA2
- RBM20
- RIT1
- RRAS
- RYR2
- SCN10A
- SCN1B
- SCN2B
- SCN3B
- SCN4B
- SCN5A
- SDHA
- SEMA3A
- SGCD
- SKI
- SLC2A10
- SLMAP
- SMAD3
- SMAD4
- SNTA1
- SOS1
- SOS2
- TAZ
- TBX20
- TCAP
- TECRL
- TGFB2
- TGFB3
- TGFBR1
- TGFBR2
- TMEM43
- TMPO
- TNNC1
- TNNI3
- TNNT2
- TPM1
- TRDN
- TRIM63
- TRPM4
- TTN
- TTR
- TXNRD2
- VCL
- ZDHHC9
EXOMAS
Alagille, síndrome
Ref. 4520
2 genes
- JAG1
- NOTCH2
EXOMAS
Sordera neurosensorial
Ref. 4579
112 genes
- ACTG1
- ADCY1
- AIFM1
- ATP2B2
- BDP1
- BSND
- CABP2
- CCDC50
- CD164
- CDC14A
- CDH23
- CEACAM16
- CIB2
- CLDN14
- CLIC5
- COCH
- COL11A2
- COL4A6
- CRYM
- DCDC2
- DIABLO
- DIAPH1
- DMXL2
- DSPP
- ELMOD3
- EPS8
- EPS8L2
- ESPN
- ESRP1
- ESRRB
- EYA4
- FAM189A2
- FOXI1
- GAB1
- GIPC3
- GJB2
- GJB3
- GJB6
- GPRASP2
- GPSM2
- GRHL2
- GRXCR1
- GRXCR2
- GSDME
- HGF
- HOMER2
- ILDR1
- KARS
- KCNJ10
- KCNQ4
- KITLG
- LHFPL5
- LOXHD1
- LRTOMT
- MARVELD2
- MCM2
- MET
- MPZL2
- MSRB3
- MYH14
- MYH9
- MYO15A
- MYO1A
- MYO3A
- MYO6
- MYO7A
- NARS2
- NLRP3
- OSBPL2
- OTOA
- OTOF
- OTOG
- OTOGL
- P2RX2
- PCDH15
- PDE1C
- PDZD7
- PJVK
- PNPT1
- POU3F4
- POU4F3
- PPIP5K2
- PRPS1
- RDX
- RIPOR2
- ROR1
- S1PR2
- SERPINB6
- SIX1
- SLC17A8
- SLC22A4
- SLC26A4
- SLC26A5
- SLC44A4
- SMPX
- STRC
- SYNE4
- TBC1D24
- TECTA
- TJP2
- TMC1
- TMEM132E
- TMIE
- TMPRSS3
- TNC
- TPRN
- TRIOBP
- TSPEAR
- USH1C
- WBP2
- WFS1
- WHRN
EXOMAS
Distrofia Muscular de Emery-Dreifuss
Ref. 4599
6 genes
- EMD
- FHL1
- LMNA
- SYNE1
- SYNE2
- TMEM43
EXOMAS
Distrofias Musculares
Ref. 4601
75 genes
- ACTA1
- AGRN
- ALG13
- ANO5
- B3GALNT2
- B3GNT2
- B4GAT1
- BVES
- CAPN3
- CAV3
- CAVIN1
- CHKB
- COL12A1
- COL6A1
- COL6A2
- COL6A3
- DAG1
- DES
- DMD
- DNAJB6
- DOK7
- DOLK
- DPAGT1
- DPM1
- DPM2
- DPM3
- DYSF
- EMD
- FAT1
- FHL1
- FKRP
- FKTN
- FLNC
- GFPT1
- GMPPB
- HNRNPDL
- INPP5K
- ISPD
- ITGA7
- ITGA9
- KLHL9
- LAMA2
- LARGE1
- LIMS2
- LMNA
- MEGF10
- MICU1
- MYOT
- PABPN1
- PLEC
- POGLUT1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- RXYLT1
- RYR1
- SELENON
- SGCA
- SGCB
- SGCD
- SGCG
- SMCHD1
- STIM1
- SYNE1
- SYNE2
- TCAP
- TMEM43
- TNPO3
- TOR1AIP1
- TRAPPC11
- TRIM32
- TRIP4
- TTN
EXOMAS
Miopatía Congénita Central Core
Ref. 4602
6 genes
- CACNA1S
- MEGF10
- MYH7
- RYR1
- SELENON
- TTN
EXOMAS
Miopatía Congénita Centronuclear
Ref. 4603
11 genes
- BIN1
- CCDC7
- CCDC78
- DNM2
- MAP3K20
- MTM1
- MTMR14
- MYF6
- RYR1
- SPEG
- TTN
EXOMAS
Enfermedades autoinflamatorias sistémicas hereditarias
Ref. 4627
29 genes
- ADA2
- ADAM17
- ADGRE2
- ARPC1B
- CARD14
- IL10
- IL10RA
- IL10RB
- IL1RN
- IL36RN
- LACC1
- LPIN2
- MEFV
- MVK
- NLRC4
- NLRP12
- NLRP3
- NOD2
- OTULIN
- PLCG2
- PSMB8
- PSTPIP1
- RBCK1
- RNF31
- TMEM173
- TNFAIP3
- TNFRSF11A
- TNFRSF1A
- WDR1
EXOMAS
Hiperinsulinemia
Ref. 4654
13 genes
- ABCC8
- CACNA1D
- GCK
- GLUD1
- HADH
- HK1
- HNF1A
- HNF4A
- INSR
- KCNJ11
- PMM2
- SLC16A1
- UCP2
EXOMAS
Síndromes Autoinflamatorios
Ref. 4676
61 genes
- ACP5
- ADA2
- ADAM17
- ADAR
- ALPI
- AP1S3
- CARD14
- CDC42
- COPA
- DNASE1L3
- DNASE2
- ELANE
- HAVCR2
- HTR1A
- IFIH1
- IL10
- IL10RA
- IL10RB
- IL1RN
- IL36RN
- LACC1
- LPIN2
- MEFV
- MVK
- NCSTN
- NLRC4
- NLRP1
- NLRP12
- NLRP3
- NLRP7
- NOD2
- OAS1
- OTULIN
- PLCG2
- POLA1
- PSMA3
- PSMB10
- PSMB4
- PSMB8
- PSMB9
- PSMG2
- PSTPIP1
- RBCK1
- RIPK1
- RNASEH2A
- RNASEH2B
- RNASEH2C
- SAMD9L
- SAMHD1
- SH3BP2
- SLC29A3
- TMEM173
- TNFAIP3
- TNFRSF11A
- TNFRSF1A
- TRAP1
- TREX1
- TRIM22
- TRNT1
- USP18
- WDR1
EXOMAS
Deficienica o insensibilidad a la hormona del crecimiento
Ref. 4680
9 genes
- BTK
- GH1
- GHR
- GHRHR
- IGF1
- IGF1R
- IGFALS
- RNPC3
- STAT5B
EXOMAS
Ceguera nocturna estacionaria congénita (CNSB)
Ref. 4686
14 genes
- CACNA1F
- GNAT1
- GNB3
- GPR179
- GRK1
- GRM6
- GUCY2D
- LRIT3
- NYX
- PDE6B
- RHO
- SAG
- SLC24A1
- TRPM1
EXOMAS
Epilepsia mioclónica
Ref. 4687
18 genes
- CACNB4
- CERS1
- CLCN2
- CSTB
- EFHC1
- EPM2A
- GABRA1
- GABRD
- GOSR2
- ICK
- KCNC1
- KCTD7
- LMNB2
- NHLRC1
- PRDM8
- PRICKLE1
- SCARB2
- TBC1D24
EXOMAS
Discapacidad Intelectual y/o Autismo + Epilepsia
Ref. 4688
87 genes
- ABAT
- ADGRG1
- ADSL
- ALDH7A1
- ALG13
- ARFGEF2
- ARHGEF9
- ARX
- ATP1A2
- CACNA1A
- CACNA1H
- CBL
- CDKL5
- CERS1
- CHD2
- CLN3
- CLN5
- CLN6
- CLN8
- CNTNAP2
- CPLX1
- CTSD
- DCX
- DNAJC5
- DNM1
- EEF1A2
- FOLR1
- FOXG1
- FOXRED1
- GABRA1
- GABRB3
- GAMT
- GATM
- GNAO1
- GRIN2A
- GRIN2B
- GRN
- HCN1
- HNRNPU
- KCNA2
- KCNQ2
- KCTD7
- LIAS
- MECP2
- MEF2C
- MFSD8
- MTHFR
- NDE1
- NDUFA1
- NDUFA11
- NDUFS1
- NDUFS3
- NDUFS4
- NDUFV1
- NEDD4L
- NRXN1
- OPHN1
- PAFAH1B1
- PCDH19
- PHF6
- PIGA
- PIGO
- PLCB1
- PNKP
- POLG
- PPT1
- RELN
- SCN1A
- SCN2A
- SCN8A
- SCN9A
- SLC2A1
- SLC9A6
- SPTAN1
- SRPX2
- ST3GAL3
- ST3GAL5
- STXBP1
- TBC1D24
- TCF4
- TSC1
- TSC2
- TSEN54
- UBE3A
- WDR62
- WWOX
- ZEB2
EXOMAS
Ectrodactilia
Ref. 4690
3 genes
- DLX5
- TP63
- WNT10B
EXOMAS
Síndrome nefrótico / FSGS
Ref. 4691
67 genes
- ACTN4
- ALG1
- ANLN
- APOL1
- ARHGAP24
- ARHGDIA
- CD151
- CD2AP
- CFH
- CLCN5
- COL4A3
- COL4A4
- COL4A5
- COQ2
- COQ6
- COQ8B
- CRB2
- CUBN
- DGKE
- E2F3
- EMP2
- FAT1
- FN1
- GPC5
- INF2
- ITGA3
- ITGB4
- KANK1
- KANK2
- KANK4
- LAGE3
- LAMB2
- LMNA
- LMX1B
- LYZ
- MAGI2
- MYH9
- MYO1E
- NPHS1
- NPHS2
- NUP107
- NUP133
- NUP160
- NUP205
- NUP85
- NUP93
- NXF5
- OCRL
- OSGEP
- PAX2
- PDSS2
- PLCE1
- PMM2
- PODXL
- PTPRO
- SCARB2
- SGPL1
- SMARCAL1
- SYNPO
- TP53RK
- TPRKB
- TRPC6
- TTC21B
- WDR73
- WT1
- XPO5
- ZMPSTE24
EXOMAS
Nefropatía hiperuricémica familiar
Ref. 4692
3 genes
- REN
- SEC61A1
- UMOD
EXOMAS
Alteraciones de la línea media / Regionalización
Ref. 4695
121 genes
- AHI1
- AMPD2
- ANOS1
- ARID1B
- ARL13B
- ARX
- ASPM
- ATR
- ATRX
- B9D1
- B9D2
- BCOR
- BMP4
- C12orf57
- CASK
- CC2D2A
- CDON
- CENPJ
- CEP152
- CEP290
- CEP41
- CEP63
- COL4A1
- CREBBP
- CTBP1
- DCX
- DHCR24
- DHCR7
- DIS3L2
- DISC1
- DISP1
- DLL1
- EFNB1
- EMX2
- EP300
- EPG5
- FGF8
- FGFR1
- FGFR2
- FH
- FKRP
- FKTN
- FLNA
- FOXH1
- GAS1
- GLI2
- GLI3
- GNRH1
- GNRHR
- GPSM2
- HCCS
- HESX1
- HS6ST1
- HYLS1
- IGBP1
- IGF1
- INPP5E
- ISPD
- KAT6B
- KIF7
- KISS1
- KISS1R
- L1CAM
- LARGE1
- LRP2
- MED12
- MID1
- MKS1
- NDE1
- NFIX
- NIN
- NODAL
- NPHP1
- NPHP3
- NSD1
- NSMF
- OFD1
- OTX2
- PAX6
- PDHA1
- PDHB
- POMGNT1
- POMGNT2
- POMT1
- POMT2
- PTCH1
- PYCR1
- RAB18
- RAB3GAP1
- RAB3GAP2
- RBBP8
- RBM10
- RELN
- RPGRIP1L
- SEMA3A
- SHH
- SIX3
- SLC12A6
- SOX2
- SPG11
- STRA6
- TAC3
- TACR3
- TCF4
- TCTN1
- TCTN2
- TCTN3
- TDGF1
- TGIF1
- TMEM138
- TMEM216
- TMEM237
- TMEM67
- TUBA1A
- TUBB2B
- TUBB3
- VAX1
- WDR11
- WDR62
- ZEB2
- ZIC2
EXOMAS
Distrofia Macular Juvenil, Enfermedad de Stargardt
Ref. 4709
13 genes
- ABCA4
- BEST1
- CTNNA1
- EFEMP1
- ELOVL4
- GUCY2D
- IMPG1
- IMPG2
- PROM1
- PRPH2
- RPGR
- RS1
- TIMP3
EXOMAS
Distrofias de retina periférica
Ref. 4711
99 genes
- ABCA4
- ADGRA3
- AGBL5
- AHR
- AIPL1
- ARHGEF18
- ARL2BP
- ARL3
- ARL6
- BBS1
- BBS2
- BEST1
- C8orf37
- CA4
- CACNA1F
- CDHR1
- CERKL
- CHM
- CLRN1
- CNGA1
- CNGB1
- CRB1
- CRX
- CYP4V2
- DHDDS
- DHX38
- EMC1
- EYS
- FAM161A
- FSCN2
- GNAT1
- GNB3
- GPR179
- GRK1
- GRM6
- GUCA1B
- GUCY2D
- HGSNAT
- HK1
- IDH3B
- IFT140
- IFT172
- IFT43
- IMPDH1
- IMPG2
- KIAA1549
- KIZ
- KLHL7
- LRAT
- LRIT3
- MAK
- MERTK
- MVK
- NEK2
- NEUROD1
- NR2E3
- NRL
- NYX
- OFD1
- PCARE
- PDE6A
- PDE6B
- PDE6G
- POMGNT1
- PRCD
- PROM1
- PRPF3
- PRPF31
- PRPF4
- PRPF6
- PRPF8
- PRPH2
- RBP3
- RDH12
- REEP6
- RGR
- RHO
- RLBP1
- ROM1
- RP1
- RP2
- RP9
- RPE65
- RPGR
- SAG
- SEMA4A
- SLC24A1
- SLC7A14
- SNRNP200
- SPATA7
- SPP2
- TOPORS
- TRNT1
- TRPM1
- TTC8
- TULP1
- USH2A
- ZNF408
- ZNF513
EXOMAS
Distrofias de retina periférica y/o centrales
Ref. 4712
61 genes
- ABCA4
- ADAM9
- AIPL1
- ALMS1
- ATF6
- C8orf37
- CABP4
- CACNA1F
- CACNA2D4
- CDHR1
- CEP290
- CEP78
- CERKL
- CFAP410
- CLUAP1
- CNGA3
- CNGB3
- CNNM4
- CRB1
- CRX
- DRAM2
- DTHD1
- ELOVL4
- EYS
- GDF6
- GNAT2
- GUCA1A
- GUCY2D
- IFT140
- IFT81
- IMPDH1
- IQCB1
- KCNJ13
- KCNV2
- LCA5
- LRAT
- NMNAT1
- OPN1LW
- OPN1MW
- OTX2
- PDE6C
- PDE6H
- PITPNM3
- POC1B
- PROM1
- PRPH2
- RAB28
- RAX2
- RD3
- RDH12
- RDH5
- RIMS1
- ROM1
- RPE65
- RPGR
- RPGRIP1
- SEMA4A
- SPATA7
- TTLL5
- TULP1
- UNC119
EXOMAS
Distrofias de retina centrales
Ref. 4713
40 genes
- ABCA4
- APOE
- ARMS2
- ATF6
- BEST1
- C2
- C3
- C9
- CFB
- CFH
- CFHR1
- CFHR3
- CFI
- CNGA3
- CNGB3
- CNNM4
- CST3
- CTNNA1
- CX3CR1
- EFEMP1
- ELOVL4
- ERCC6
- FBLN5
- GNAT2
- GUCY2D
- HMCN1
- HTRA1
- IMPG1
- IMPG2
- OPN1LW
- OPN1MW
- OPN1SW
- PDE6C
- PDE6H
- PROM1
- PRPH2
- RAX2
- RPGR
- RS1
- TIMP3
EXOMAS
Senior-Loken, Síndrome
Ref. 4754
7 genes
- CEP290
- IQCB1
- NPHP1
- NPHP4
- SDCCAG8
- TRAF3IP1
- WDR19
EXOMAS
Distrofinopatías
Ref. 4766
1 genes
- DMD
EXOMAS
Coffin-Siris-Like, Síndrome
Ref. 10046
26 genes
- ADNP
- ANKRD11
- ARID1A
- ARID1B
- ARID2
- BRD4
- DPF2
- HDAC8
- NIPBL
- PACS1
- PHF6
- PIGV
- RAD21
- SMARCA2
- SMARCA4
- SMARCB1
- SMARCC2
- SMARCD1
- SMARCE1
- SMC1A
- SMC3
- SOX11
- SOX4
- STAG1
- STAG2
- TBC1D24
EXOMAS
Malformaciones cerebrales
Ref. 10047
220 genes
- ACTB
- ACTG1
- ADGRG1
- AHI1
- AKT3
- AMPD2
- ANKLE2
- ANOS1
- ARFGEF2
- ARID1B
- ARL13B
- ARX
- ASPM
- ATR
- ATRIP
- ATRX
- B9D1
- B9D2
- BCOR
- BMP4
- C12orf57
- C7orf43
- CASK
- CC2D2A
- CDC45
- CDC6
- CDK5
- CDK5RAP2
- CDK6
- CDKL5
- CDON
- CDT1
- CENPE
- CENPJ
- CEP135
- CEP152
- CEP290
- CEP41
- CEP63
- CHD7
- CHMP1A
- CIT
- CLP1
- COASY
- COL18A1
- COL4A1
- COPB2
- CREBBP
- CTBP1
- CTNNA2
- DCHS1
- DCX
- DEPDC5
- DHCR24
- DHCR7
- DIS3L2
- DISC1
- DISP1
- DLL1
- DYNC1H1
- EFNB1
- EMX2
- EOMES
- EP300
- EPG5
- ERMARD
- EXOSC3
- EXOSC8
- EXOSC9
- EZH2
- FAT4
- FGF8
- FGFR1
- FGFR2
- FH
- FIG4
- FKRP
- FKTN
- FLNA
- FMR1
- FOXG1
- FOXH1
- GAS1
- GLI2
- GLI3
- GMNN
- GNRH1
- GNRHR
- GPSM2
- HCCS
- HESX1
- HS6ST1
- HYLS1
- IER3IP1
- IGBP1
- IGF1
- INPP5E
- ISPD
- KAT6B
- KATNB1
- KIF14
- KIF1BP
- KIF2A
- KIF5C
- KIF7
- KISS1
- KISS1R
- KNL1
- L1CAM
- LAMB1
- LARGE1
- LRP2
- MCM5
- MCPH1
- MECP2
- MED12
- MED17
- MFSD2A
- MID1
- MKS1
- MTOR
- MYCN
- NCAPD2
- NCAPD3
- NCAPH
- NDE1
- NFIX
- NIN
- NODAL
- NPHP1
- NPHP3
- NPRL3
- NSD1
- NSDHL
- NSMF
- NUP37
- OCLN
- OFD1
- ORC1
- ORC4
- ORC6
- OTX2
- PAFAH1B1
- PAX6
- PCLO
- PCNT
- PDHA1
- PDHB
- PHC1
- PIK3CA
- PIK3R2
- PNKP
- POMGNT1
- POMGNT2
- POMT1
- POMT2
- PTCH1
- PYCR1
- RAB18
- RAB3GAP1
- RAB3GAP2
- RARS2
- RBBP8
- RBM10
- RELN
- RPGRIP1L
- RTTN
- SASS6
- SEMA3A
- SEPSECS
- SHH
- SIX3
- SLC12A6
- SLC25A19
- SLC2A1
- SLC9A6
- SNAP29
- SOX2
- SPG11
- SRPX2
- STIL
- STRA6
- TAC3
- TACR3
- TBC1D20
- TBC1D23
- TCF4
- TCTN1
- TCTN2
- TCTN3
- TDGF1
- TGIF1
- TMEM138
- TMEM216
- TMEM237
- TMEM67
- TMTC3
- TOE1
- TSEN15
- TSEN2
- TSEN34
- TSEN54
- TUBA1A
- TUBA8
- TUBB
- TUBB2A
- TUBB2B
- TUBB3
- TUBG1
- UBE3A
- VAX1
- VLDLR
- VPS53
- VRK1
- WDFY3
- WDR11
- WDR62
- ZEB2
- ZIC2
- ZNF335