polycystic kidney, type 1 autosomal dominant disease

Preferred Label : polycystic kidney, type 1 autosomal dominant disease;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0355414;

UMLS CUI

C0887850;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis [ICD-11 More detail]
Currated CISMeF NLP mapping
- Autosomal Dominant Polycystic Kidney Disease Type I [NCIt concept]
Related record
- polycystic kidney, autosomal dominant [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adult type polycystic kidney disease type 1 (disorder) [SNOMED CT concept]
- Autosomal Dominant Polycystic Kidney Disease Type I [NCIt concept]
- Polycystic liver disease 1 with or without kidney cysts [OMIM Phenotype]