Autosomal dominant polycystic liver disease

ICD-10 Code Q44.6

Autosomal dominant polycystic liver disease

Definition

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

Also known as AD polycystic liver disease, ADPLD, isolated congenital polycystic liver disease, isolated polycystic liver disease, PCLD, polycystic liver disease — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Alimentary part of gastrointestinal system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Alimentary part of gastrointestinal system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Liver Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Liver Disease Has Primary Anatomic Site NCIT · CC BY 4.0