ATP binding cassette subfamily A member 1

Preferred Label : ATP binding cassette subfamily A member 1;

Approved symbol HGNC : ABCA1;

Name synonyms HGNC : Tangier disease;

Alias symbols HGNC : TGD;

Chromosome HGNC : 9q31.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000165029;

Details

Origin ID

HGNC:29;

UMLS CUI

C1412058;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily A member 1 [ORDO Gene]
- Analphalipoproteinaemia [ICD-11 More detail]
- Atp-binding cassette, subfamily a, member 1 [OMIM gene]
- Lipoprotein deficiency [ICD-10 Sub-category]
- Phospholipid-Transporting ATPase ABCA1 [NCIt concept]
- Tangier Disease [NCIt concept]
- Tangier disease [OMIM Phenotype]
- Tangier disease [ORDO Disease]
- Tangier disease [MedDRA Preferred Term]
- Tangier disease [DO Concept]
- Tangier disease (disorder) [SNOMED CT concept]
- tangier disease [MeSH concept]
- tangier disease [MeSH Descriptor]
NCIt concept
- ABCA1 Gene [NCIt concept]
OMIM gene
- Atp-binding cassette, subfamily a, member 1 [OMIM gene]
Orphanet gene
- ATP binding cassette subfamily A member 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ABCA1 Gene [NCIt concept]
- ATP binding cassette subfamily A member 1 [ORDO Gene]
- Atp-binding cassette, subfamily a, member 1 [OMIM gene]

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