DMD Gene - CISMeF

Preferred Label : DMD Gene;

NCIt synonyms : DMD; Dystrophin (Muscular Dystrophy, Duchenne And Becker Types) Gene;

CISMeF acronym : DMD;

NCIt definition : This gene is involved in muscle development.;

Details

Origin ID

C75324;

UMLS CUI

C1414083;

Automatic exact mappings (from CISMeF team)
- DMD gene [LOINC component]
- Duchenne muscular dystrophy (disorder) [SNOMED CT concept]
- Dystrophin [OMIM gene]
- Muscular dystrophy, duchenne type [OMIM Phenotype]
- dystrophin [ORDO Gene]
- muscular dystrophy, duchenne [MeSH Descriptor]
False automatic mappings
- Duchenne muscular dystrophy [ORDO Disease]
HGNC gene
- dystrophin [HGNC gene]
OMIM relation
- Dystrophin [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DMD gene [LOINC component]
- Dystrophin [OMIM gene]
- dystrophin [HGNC gene]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Reference Gene Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_encodes_gene_product
- Dystrophin [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_mapped_to_disease
- Becker's Muscular Dystrophy [NCIt concept]
- Duchenne Muscular Dystrophy [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Organogenesis [NCIt concept]
- Regulation of Cell Shape [NCIt concept]
genetic_biomarker_related_to
- Dystrophin Actual to Control Ratio Measurement [NCIt concept]
- Dystrophin Measurement [NCIt concept]
- IL1RAPL1/DMD Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

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