Glycogen phosphorylase, muscle

Preferred Label : Glycogen phosphorylase, muscle;

Symbol : PYGM;

CISMeF acronym : PYGM;

Type : Gene;

Alternative titles and symbols : MYOPHOSPHORYLASE;

Ensembl ID : ENSG00000068976;

Prefixed ID : *608455;

Details

Origin ID

608455;

UMLS CUI

C1419157;

Automatic exact mappings (from CISMeF team)
- 1,4-alpha-oligoglucan phosphorylase activity [GO term]
- PYGM gene [LOINC component]
- glycogen phosphorylase, muscle associated [ORDO Gene]
- glycogen phosphorylase, muscle associated [HGNC gene]
- glycogen phosphorylase, muscle form [MeSH Descriptor]
HGNC gene
- glycogen phosphorylase, muscle associated [HGNC gene]
NCIt concept(s)
- Glycogen Phosphorylase, Muscle Form [NCIt concept]
- PYGM Gene [NCIt concept]
- PYGM wt Allele [NCIt concept]
ORDO concept(s)
- glycogen phosphorylase, muscle associated [ORDO Gene]
Phenotypes related
- Glycogen storage disease V [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PYGM gene [LOINC component]
- glycogen phosphorylase, muscle associated [HGNC gene]

Keyword's position in hierarchy(ies) :

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