Dystrophin - CISMeF

Preferred Label : Dystrophin;

Symbol : DMD;

CISMeF acronym : DMD;

Type : Gene;

Included titles and symbols : Apo-dystrophin 1;

Ensembl ID : ENSG00000198947;

Prefixed ID : *300377;

Details

Origin ID

300377;

UMLS CUI

C1414083;

Automatic exact mappings (from CISMeF team)
- DMD Gene [NCIt concept]
- DMD gene [LOINC component]
- Doctor of Dental Medicine [NCIt concept]
- Duchenne muscular dystrophy [ORDO Disease]
- Duchenne muscular dystrophy (disorder) [SNOMED CT concept]
- Dystrophin [NCIt concept]
- Dystrophin [FMA entity]
- apo-dystrophin 1 [MeSH concept]
- apo-dystrophin 1 [MeSH Supplementary Concept]
- dystrophin [ORDO Gene]
- dystrophin [MeSH Descriptor]
- dystrophin [MeSH concept]
- dystrophin [HGNC gene]
- muscular dystrophy, duchenne [MeSH Descriptor]
HGNC gene
- dystrophin [HGNC gene]
NCIt concept(s)
- DMD Gene [NCIt concept]
- DMD wt Allele [NCIt concept]
- Dystrophin [NCIt concept]
ORDO concept(s)
- dystrophin [ORDO Gene]
Phenotypes related
- Cardiomyopathy, dilated, 3b [OMIM Phenotype]
- Muscular dystrophy, becker type [OMIM Phenotype]
- Muscular dystrophy, duchenne type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DMD Gene [NCIt concept]
- DMD gene [LOINC component]
- dystrophin [HGNC gene]

Keyword's position in hierarchy(ies) :

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