Mitochondrial fission factor

Preferred Label : Mitochondrial fission factor;

Symbol : MFF;

CISMeF acronym : MFF;

Type : Gene;

Alternative titles and symbols : Chromosome 2 open reading frame 33; C2ORF33;

Ensembl ID : ENSG00000168958;

Prefixed ID : *614785;

Details

Origin ID

614785;

UMLS CUI

C1540223;

Automatic exact mappings (from CISMeF team)
- MFF Gene [NCIt concept]
- MFF wt Allele [NCIt concept]
- Mitochondrial Fission Factor [NCIt concept]
- mitochondrial fission factor [ORDO Gene]
- mitochondrial fission factor [HGNC gene]
HGNC gene
- mitochondrial fission factor [HGNC gene]
NCIt concept(s)
- MFF Gene [NCIt concept]
- MFF wt Allele [NCIt concept]
- Mitochondrial Fission Factor [NCIt concept]
ORDO concept(s)
- mitochondrial fission factor [ORDO Gene]
Phenotypes related
- Encephalopathy due to defective mitochondrial and peroxisomal fission 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MFF Gene [NCIt concept]
- mitochondrial fission factor [HGNC gene]

Keyword's position in hierarchy(ies) :

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