cirrhosis, familial

Preferred Label : cirrhosis, familial;

Origin ID

C566123;

UMLS CUI

C1861556;

Automatic exact mappings (from CISMeF team)
- Cirrhosis, familial [OMIM Phenotype]
Currated CISMeF NLP mapping
- Cirrhosis, familial [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, inborn [MeSH Descriptor]
- liver cirrhosis [MeSH Descriptor]
Record concept(s)
- cirrhosis, familial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cirrhosis, familial [OMIM Phenotype]
- Cirrhosis, familial [OMIM Phenotype]