north american indian childhood cirrhosis

Preferred Label : north american indian childhood cirrhosis;

Origin ID

C565737;

UMLS CUI

C1858051;

Automatic exact mappings (from CISMeF team)
- North American Indian childhood cirrhosis (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hereditary North American Indian childhood cirrhosis [ORDO Disease]
- North american indian childhood cirrhosis [OMIM Phenotype]
MeSH term(s) associated for indexing
- liver cirrhosis, biliary [MeSH Descriptor]
Record concept(s)
- north american indian childhood cirrhosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary North American Indian childhood cirrhosis [ORDO Disease]
- North American Indian childhood cirrhosis (disorder) [SNOMED CT concept]
- North american indian childhood cirrhosis [OMIM Phenotype]