Autosomal recessive polycystic kidney disease
MONDO:0009889An 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, 6 tagged with Autosomal recessive polycystic kidney disease itself.
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Browse by category →Sub-types of Autosomal recessive polycystic kidney disease
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Polycystic kidney disease 4 0 trials
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Polycystic kidney disease 5 0 trials