Cirrhosis, familial

Preferred Label : Cirrhosis, familial;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? Autosomal dominant;

Prefixed ID : 118900;

Details

Origin ID

118900;

UMLS CUI

C1861556;

Currated CISMeF NLP mapping
- cirrhosis, familial [MeSH concept]
- cirrhosis, familial [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Chronic active hepatitis [HPO term]
- Cirrhosis [HPO term]
- Hepatitis [HPO term]
- Increased circulating antibody level [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cirrhosis, familial [MeSH Supplementary Concept]
- cirrhosis, familial [MeSH concept]

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