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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
polycystic kidney disease 1  
polycystic kidney disease 2  
polycystic kidney disease 3  
Polycystic Kidney Disease 6 with or without Polycystic Liver Disease  
Polycystic Kidney Disease 7  
An autosomal dominant nephropathy characterized by the development of small kidney cysts and renal interstitial fibrosis causing adult-onset progressive loss of kidney function leading to end-stage kidney disease after around 60 years of age. Caused by heterozygous mutation in the ALG5 gene on chromosome 13q13.

Synonyms
Exact Synonyms: PKD7
Primary IDs: OMIM:620056
Definition Sources: OMIM:620056

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