ATP binding cassette subfamily A member 4

Preferred Label : ATP binding cassette subfamily A member 4;

Approved symbol HGNC : ABCA4;

Name synonyms HGNC : Stargardt disease;

Alias symbols HGNC : ARMD2; CORD3; FFM;

Chromosome HGNC : 1p22.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000198691;

Details

Origin ID

HGNC:34;

UMLS CUI

C1412063;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily A member 4 [ORDO Gene]
- Atp-binding cassette, subfamily a, member 4 [OMIM gene]
- Macular degeneration, age-related, 2 [OMIM Phenotype]
- Stargardt Disease [NCIt concept]
- Stargardt Disease [MeSH concept]
- Stargardt Disease [MeSH Descriptor]
- Stargardt disease [ICD-11 More detail]
- Stargardt disease [ORDO Disease]
- Stargardt disease [DO Concept]
- Stargardt's disease [MedDRA Preferred Term]
- Stargardt's disease (disorder) [SNOMED CT concept]
- stargardt's disease [SNOMED Notion]
OMIM gene
- Atp-binding cassette, subfamily a, member 4 [OMIM gene]
Orphanet gene
- ATP binding cassette subfamily A member 4 [ORDO Gene]
See also inter- (CISMeF)
- Cone-rod dystrophy 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Atp-binding cassette, subfamily a, member 4 [OMIM gene]

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