Tubulointerstitial and metabolic diseases

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Showing 13–24 of 24 results

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Joubert syndrome [34 genes]

Ref.: S-202110429

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Liddle syndrome (pseudohyperaldosteronism) [7 genes]

Ref.: S-202008455

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Meckel-Gruber syndrome [20 genes]

Ref.: S-202110430

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Metabolic alkalosis [25 genes]

Ref.: S-202110414

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Nephrogenic diabetes insipidus (NDI) [3 genes]

Ref.: S-202008443

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Nephronophthisis [36 genes]

Ref.: S-202110423

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Polycystic kidney disease [22 genes]

Ref.: S-202110426

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Primary hyperoxaluria [3 genes]

Ref.: S-201906671

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Primary xanthinuria [2 genes]

Ref.: S-202110432

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Renal tubular acidosis (RTA) [29 genes]

Ref.: S-202008439

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Senior-Løken syndrome [15 genes]

Ref.: S-202313097

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Tubulointerstitial and metabolic diseases [283 genes]

Ref.: S-202110419