Search Ontology:
Human Disease

autosomal dominant polycystic kidney disease

Term ID
DOID:898
Synonyms
  • ADPKD
  • Congenital biliary ectasias
  • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Definition
A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal dominant fashion. (3)
References
  • GARD:10413
  • ICD10CM:Q61.3
  • ICD9CM:753.12
  • MESH:D007690
  • NCI:C75464
  • ORDO:730
  • SNOMEDCT_US_2023_03_01:204955006
  • UMLS_CUI:C0022680
Ontology
Human Disease   ( DOID:898 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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