Autosomal recessive polycystic kidney disease

MONDO:0009889

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

Also known as: AR-PKD, ARPKD, autosomal recessive polycystic kidney, polycystic kidney disease, autosomal recessive, polycystic kidney disease, infantile type, polycystic kidney and hepatic disease 1, polycystic kidney disease, infantile, type I, PKHD1

7 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by