Fatty acid 2-hydroxylase

Preferred Label : Fatty acid 2-hydroxylase;

Symbol : FA2H;

CISMeF acronym : FA2H;

Type : Gene;

Alternative titles and symbols : Fatty acid alpha-hydroxylase; Fatty acid hydroxylase domain-containing protein 1; Fah1, s. cerevisiae, homolog of; Scs7, s. cerevisiae, homolog of; FAAH; FAXDC1; FAH1; SCS7;

Ensembl ID : ENSG00000103089;

Prefixed ID : *611026;

Détails

Origin ID

611026;

UMLS CUI

C1427405;

Automatic exact mappings (from CISMeF team)
- Fatty Acid 2-Hydroxylase [NCIt concept]
- fatty acid alpha-hydroxylase [MeSH concept]
- fatty acid alpha-hydroxylase [MeSH Supplementary Concept]
- fatty acid alpha-hydroxylase activity [GO term]
Currated CISMeF NLP mapping
- FA2H Gene [NCIt concept]
- fatty acid 2-hydroxylase [ORDO Gene]
- fatty acid 2-hydroxylase [HGNC gene]
HGNC gene
- fatty acid 2-hydroxylase [HGNC gene]
NCIt concept(s)
- FA2H Gene [NCIt concept]
- FA2H wt Allele [NCIt concept]
- Fatty Acid 2-Hydroxylase [NCIt concept]
ORDO concept(s)
- fatty acid 2-hydroxylase [ORDO Gene]
Phenotypes related
- Spastic paraplegia 35, autosomal recessive, with or without neurodegeneration [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FA2H Gene [NCIt concept]
- fatty acid 2-hydroxylase [HGNC gene]
Validated automatic mappings to BTNT
- FA2H wt Allele [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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