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DO Term : autosomal recessive polycystic kidney disease [DOID:0110861] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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 recessive fashion.
  • synonyms:
  • NCI:C84579,
  • GARD:8378,
  • MESH:D017044,
  • UMLS_CUI:C0085548,
  • ICD10CM:Q61.1,
  • ORDO:731,
  • AR-PKD,
  • SNOMEDCT_US_2023_03_01:28770003,
  • ICD9CM:753.14
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents