glycogen storage disease IIIA

Preferred Label : glycogen storage disease IIIA;

MeSH note : PROM mutation in glycogen debrancher enzyme;

MeSH synonym : GSD IIIA;

Origin ID

C566889;

UMLS CUI

C1968739;

Automatic exact mappings (from CISMeF team)
- Glycogen storage disease III [OMIM Phenotype]
CISMeF manual mappings
- glycogen storage disease type 3a [Disease (Nov.)]
MeSH term(s) associated for indexing
- glycogen storage disease type iii [MeSH Descriptor]
Record concept(s)
- glycogen storage disease IIIA [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- glycogen storage disease type 3a [Disease (Nov.)]
Validated automatic mappings to NTBT
- Glycogen storage disease type III [MedDRA Preferred Term]