An instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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thiopurine metabolic disease
MONDO:0000210
hypercalcemia, infantile
MONDO:0000212
hypermanganesemia with dystonia
MONDO:0000214
polycystic echinococcosis
MONDO:0000288
autosomal dominant polycystic liver disease
MONDO:0000447
abdominal obesity-metabolic syndrome
MONDO:0000816