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SEC61B-related polycystic liver disease

MONDO:0550003

Any autosomal dominant polycystic liver disease in which the cause of the disease is a mutation in the SEC61B gene.

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

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Broader categories

Disease (717) Liver disorder (316) Hereditary disease (188) Digestive system disorder (166) Endocrine system disorder (78) Human disease (15) Hepatobiliary disorder (10) Autosomal dominant polycystic liver disease (3) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0)

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