chromosome 19 open reading frame 12

Preferred Label : chromosome 19 open reading frame 12;

Approved symbol HGNC : C19orf12;

Name synonyms HGNC : neurodegeneration with brain iron accumulation 4; membrane protein-associated neurodegeneration;

Alias symbols HGNC : NBIA4; MGC10922; MPAN; DKFZP762D096;

Chromosome HGNC : 19q12;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000131943;

Details

Origin ID

HGNC:25443;

UMLS CUI

C1428487;

Automatic exact mappings (from CISMeF team)
- Chromosome 19 open reading frame 12 [OMIM gene]
- Mitochondrial membrane protein associated neurodegeneration (disorder) [SNOMED CT concept]
- Neurodegeneration with Brain Iron Accumulation 4 [NCIt concept]
- Neurodegeneration with brain iron accumulation 4 [OMIM Phenotype]
- chromosome 19 open reading frame 12 [ORDO Gene]
- neurodegeneration with brain iron accumulation 4 [DO Concept]
NCIt concept
- C19orf12 Gene [NCIt concept]
Orphanet gene
- chromosome 19 open reading frame 12 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- C19orf12 Gene [NCIt concept]
- Chromosome 19 open reading frame 12 [OMIM gene]

Keyword's position in hierarchy(ies) :

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