Unc119 lipid-binding chaperone

Preferred Label : Unc119 lipid-binding chaperone;

Symbol : UNC119;

CISMeF acronym : HRG4; UNC119;

Type : Gene and phenotype, combined;

Alternative titles and symbols : Human retinal gene 4; HRG4; Unc119, C. elegans, homolog of;

Included titles and symbols : Cone-rod dystrophy;

Prefixed ID : 604011;

Details

Origin ID

604011;

UMLS CUI

C1421355;

Automatic exact mappings (from CISMeF team)
- Cone-Rod Dystrophies [MeSH Descriptor]
- Cone-Rod Dystrophies [MeSH concept]
- Protein Unc-119 Homolog A [NCIt concept]
- UNC119 Gene [NCIt concept]
- UNC119 wt Allele [NCIt concept]
- cone-rod dystrophy [DO Concept]
- retinitis pigmentosa [MeSH Descriptor]
- unc-119 lipid binding chaperone [HGNC gene]
Currated CISMeF NLP mapping
- unc-119 lipid binding chaperone [ORDO Gene]
NCIt concept(s)
- Protein Unc-119 Homolog A [NCIt concept]
- UNC119 Gene [NCIt concept]
- UNC119 wt Allele [NCIt concept]
ORDO concept(s)
- unc-119 lipid binding chaperone [ORDO Gene]
See also inter- (CISMeF)
- cone rod dystrophy [Disease (Nov.)]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- UNC119 Gene [NCIt concept]
- unc-119 lipid binding chaperone [ORDO Gene]
- unc-119 lipid binding chaperone [HGNC gene]

Keyword's position in hierarchy(ies) :

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