Huntingtin - CISMeF

Preferred Label : Huntingtin;

Symbol : HTT;

CISMeF acronym : HTT;

Type : Gene;

Alternative titles and symbols : Hd gene; IT15;

Ensembl ID : ENSG00000197386;

Prefixed ID : *613004;

Details

Origin ID

613004;

UMLS CUI

C1415504;

Automatic exact mappings (from CISMeF team)
- HTT Gene [NCIt concept]
- HTT gene [LOINC component]
- HTT wt Allele [NCIt concept]
- Huntingtin [NCIt concept]
- SLC6A4 wt Allele [NCIt concept]
- Thyroid Gland Hyalinizing Trabecular Tumor [NCIt concept]
- huntingtin [ORDO Gene]
- huntingtin [HGNC gene]
- symbol withdrawn HTT [HGNC gene]
HGNC gene
- symbol withdrawn HTT [HGNC gene]
NCIt concept(s)
- HTT Gene [NCIt concept]
- HTT wt Allele [NCIt concept]
- Huntingtin [NCIt concept]
ORDO concept(s)
- huntingtin [ORDO Gene]
Phenotypes related
- Huntington disease [OMIM Phenotype]
- Lopes-maciel-rodan syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HTT Gene [NCIt concept]
- HTT gene [LOINC component]
- huntingtin [HGNC gene]

Keyword's position in hierarchy(ies) :

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