Dystonin - CISMeF

Preferred Label : Dystonin;

Symbol : DST;

CISMeF acronym : DST;

Type : Gene;

Alternative titles and symbols : Dystonia musculorum, mouse, homolog of; Bullous pemphigoid antigen 1; DMH; DT; BPAG1; BP240; BP230;

Ensembl ID : ENSG00000151914;

Prefixed ID : *113810;

Details

Origin ID

113810;

UMLS CUI

C1539312;

Automatic exact mappings (from CISMeF team)
- 1,2-Dimethylhydrazine [NCIt concept]
- DMH [MeSH concept]
- DST Gene [NCIt concept]
- DST wt Allele [NCIt concept]
- Daylight-Savings Time [NCIt concept]
- Device Tracking and Disposition Domain [NCIt concept]
- Digital Tomosynthesis [NCIt concept]
- Diphtheria Toxoid/Tetanus Toxoid Vaccine Adsorbed [NCIt concept]
- Domestic medium-haired cat (organism) [SNOMED CT concept]
- Dystonin [MeSH Descriptor]
- Dystonin [NCIt concept]
- Dystonin [MeSH concept]
- GDC Disease Type Terminology [NCIt concept]
- L-Dopachrome Tautomerase [NCIt concept]
- Thymidine [NCIt concept]
- dentatothalamic tract [UBERON concept]
- dorsomedial nucleus of hypothalamus [UBERON concept]
- drug therapy [MeSH Descriptor]
- dystonin [ORDO Gene]
- dystonin [HGNC gene]
False automatic mappings
- dimenhydrinate [MeSH Descriptor]
HGNC gene
- dystonin [HGNC gene]
NCIt concept(s)
- DST Gene [NCIt concept]
- DST wt Allele [NCIt concept]
- Dystonin [NCIt concept]
ORDO concept(s)
- dystonin [ORDO Gene]
Phenotypes related
- Epidermolysis bullosa simplex 3, localized or generalized intermediate, with bp230 deficiency [OMIM Phenotype]
- Neuropathy, hereditary sensory and autonomic, type VI [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DST Gene [NCIt concept]
- dystonin [HGNC gene]

Keyword's position in hierarchy(ies) :

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