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DO Term : autosomal dominant polycystic kidney disease [DOID:898] 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 dominant fashion.

synonyms:
SNOMEDCT_US_2023_03_01:204955006,
MESH:D007690,
ICD9CM:753.12,
NCI:C75464,
UMLS_CUI:C0022680,
ICD10CM:Q61.3,
ORDO:730,
Congenital biliary ectasias,
ADPKD,
GARD:10413,
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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