ALG8-related autosomal dominant polycystic kidney and/or liver disease

MONDO:1060122

An autosomal dominant disease caused by variants in the ALG8 gene that is characterized by incomplete penetrance and a range of clinical manifestations, spanning from individuals with normal kidneys to those with numerous kidney cysts and chronic kidney disease (CKD). While the common presentation involves a limited number of kidney cysts and maintained kidney function, severe polycystic liver disease (PLD) with minimal kidney involvement (ADPLD) can also occur.

Also known as: ADPKLD-ALG8, autosomal dominant polycystic kidney and/or liver disease-ALG8

0 clinical trials for this condition and its sub-types, 0 tagged with ALG8-related autosomal dominant polycystic kidney and/or liver disease itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant disease (699)

Including sub-types (0) Tagged with ALG8-related autosomal dominant polycystic kidney and/or liver disease (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.