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cirrhosis, familial | RareConnect | RareConnect.io

/hereditary disease

/cirrhosis of liver

/telomere syndrome

/cirrhosis, familial

cirrhosis, familial

Rare Disease

MONDO:0007329

Also Known As

cirrhosis, familialcryptogenic cirrhosishereditary cirrhosis of liverIndian childhood cirrhosisSen syndromecirrhosis, Noncryptogenic, susceptibility tocirrhosis, cryptogeniccirrhosis, familial, with pulmonary hypertensioncopper toxicosis, idiopathiccopper-overload cirrhosisendemic Tyrolean infantile cirrhosis

Definition

Cirrhosis in which no causative agent can be identified.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:215600 ↗

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