amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase

Preferred Label : amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase;

Approved symbol HGNC : AGL;

Name synonyms HGNC : glycogen storage disease type III; glycogen debranching enzyme;

Alias symbols HGNC : GDE;

Chromosome HGNC : 1p21.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000162688;

Details

Origin ID

HGNC:321;

UMLS CUI

C1412279;

Automatic exact mappings (from CISMeF team)
- Amylo-1,6-glucosidase, 4-alpha-glucanotransferase [OMIM gene]
- Glycogen Storage Disease Type III [NCIt concept]
- Glycogen storage disease due to glycogen debranching enzyme deficiency [ORDO Disease]
- Glycogen storage disease type III [MedDRA Preferred Term]
- Glycogen storage disease, type III (disorder) [SNOMED CT concept]
- amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase [ORDO Gene]
- glycogen debranching enzyme [MeSH concept]
- glycogen debranching enzyme system [MeSH Descriptor]
- glycogen storage disease III [DO Concept]
- glycogen storage disease type III [MeSH concept]
- glycogen storage disease type iii [MeSH Descriptor]
- glycogen storage disease, type iii [SNOMED Notion]
OMIM gene
- Amylo-1,6-glucosidase, 4-alpha-glucanotransferase [OMIM gene]
Orphanet gene
- amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- AGL gene [LOINC component]
- Amylo-1,6-glucosidase, 4-alpha-glucanotransferase [OMIM gene]

Keyword's position in hierarchy(ies) :

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