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Up to: Autosomal dominant medullary cystic kidney disease with or without hyperuricemia · Familial juvenile hyperuricemic nephropathy
Tubulointerstitial kidney disease, autosomal dominant, 2
An inherited disorder that causes a gradual loss of kidney function, caused by a mutation in the MUC1 gene that leads to production of an abnormal mucin 1 protein, which deposits in the kidney and leads to slow loss of kidney function.
This condition has no sub-types.