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Autosomal dominant polycystic liver disease

rare

An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver.

Identifiers: MONDO:0000447 Orphanet:2924
Part of: Autosomal dominant disease Liver disorder
Also known as: AD polycystic liver disease · ADPLD · isolated congenital polycystic liver disease · isolated polycystic liver disease · PCLD

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
SEC61B-related polycystic liver disease	MONDO:0550003		SEC61B
Polycystic liver disease 1	MONDO:0008265		PRKCSH
Polycystic liver disease 2	MONDO:0014860		SEC63
Polycystic liver disease 3 with or without kidney cysts	MONDO:0054743		ALG8
Polycystic liver disease 4 with or without kidney cysts	MONDO:0044327		LRP5

Rare disease

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