Autosomal recessive polycystic kidney disease

rare

An inherited disorder characterized by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involvement.

Identifiers: MONDO:0009889 Orphanet:731
Part of: Autosomal recessive disease Polycystic kidney disease
Also known as: AR-PKD · ARPKD · autosomal recessive polycystic kidney · PKHD1 · polycystic kidney disease, autosomal recessive

Subtypes

Disease	ID	Subtypes	Genes
Polycystic kidney disease 4	MONDO:0033004		PKHD1
Polycystic kidney disease 5	MONDO:0033281		DZIP1L

Rare disease

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