cirrhosis, familial, with deposition of abnormal glycogen

Preferred Label : cirrhosis, familial, with deposition of abnormal glycogen;

Origin ID

C537275;

UMLS CUI

C2936914;

Automatic exact mappings (from CISMeF team)
- Glycogen storage disease iv [OMIM Phenotype]
MeSH term(s) associated for indexing
- glycogen storage disease type iv [MeSH Descriptor]
Record concept(s)
- Cirrhosis, familial, with deposition of abnormal glycogen [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]