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Renal cysts and diabetes syndrome

^ http://www.orpha.net/ORDO/Orphanet_93111


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.

Synonyms: HNF1B-MODY, RCAD syndrome, MODY5, Renal dysfunction-early-onset diabetes syndrome, Renal cysts-maturity-onset diabetes of the young syndrome, HNF1B-related renal cysts and diabetes syndrome

Term info

database cross reference
  • ICD-10:E11.2 (Attributed)
  • OMIM:616026 (BTNT (broader term maps to a narrower term))
  • ICD-10:E11.2 (NTBT (narrower term maps to a broader term))
  • UMLS:C2959918 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C0431693 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:C535520 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:137920 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

OMIM:616026, MeSH:C535520, UMLS:C0431693, UMLS:C2959918, ICD-10:E11.2, OMIM:137920

notation

ORPHA:93111