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Renal cysts and diabetes syndrome
rareRenal cysts and diabetes syndrome (RCAD) is a rare form of maturity-onset diabetes of the young (MODY) characterized clinically by heterogeneous cystic renal disease and early-onset familial non-autoimmune diabetes. Pancreatic atrophy, liver dysfunction and genital tract anomalies are also features of the syndrome.
- Identifiers
- MONDO:0007669 OMIM:137920Orphanet:93111
- Causal genes
- HNF1B
- Part of
- Familial juvenile hyperuricemic nephropathyMaturity-onset diabetes of the youngSyndromic disease
- Also known as
- CAKUT with diabetes · congenital anomalies of the kidney and urinary tract with diabetes · FJHN atypical · hepatocyte nuclear Factor 1-beta-associated monogenic diabetes · HNF1B-MODY
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