apoptosis inducing factor mitochondria associated 1

Preferred Label : apoptosis inducing factor mitochondria associated 1;

Approved symbol HGNC : AIFM1;

Alias symbols HGNC : CMTX4; DFNX5; AIF;

Chromosome HGNC : Xq26.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000156709;

Details

Origin ID

HGNC:8768;

UMLS CUI

C1826618;

Automatic exact mappings (from CISMeF team)
- Apoptosis-inducing factor, mitochondria-associated, 1 [OMIM gene]
- Charcot-marie-tooth disease, X-linked recessive, 4, with or without cerebellar ataxia [OMIM Phenotype]
- Deafness, X-linked 5, with peripheral neuropathy [OMIM Phenotype]
- apoptosis inducing factor mitochondria associated 1 [ORDO Gene]
NCIt concept
- AIFM1 Gene [NCIt concept]
OMIM gene
- Apoptosis-inducing factor, mitochondria-associated, 1 [OMIM gene]
Orphanet gene
- apoptosis inducing factor mitochondria associated 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- AIFM1 Gene [NCIt concept]
- Apoptosis-inducing factor, mitochondria-associated, 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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