|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Renal cysts and diabetes syndrome (RCAD) is a rare form of maturity-onset diabetes of the young (MODY; see this term) 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. (Orphanet Rare Disease Ontology, Orphanet_93111)|
|Downloads & Tools|
1 genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset.
|HNF1B||HNF1 homeobox B||2.88009|