Muscular dystrophy

Preferred Label : Muscular dystrophy;

Origin ID

T00754;

Automatic exact mappings (from CISMeF team)
- dystrophin [HGNC gene]
- neurological disease other [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- MUSCULAR DYSTROPHY [WHO-ART Included Term]
- Muscular Dystrophy [NCIt concept]
- Muscular dystrophy [ORDO Disease]
- Muscular dystrophy [HPO term]
- Muscular dystrophy [PASCAL descriptor]
- Muscular dystrophy [ICD-10 Sub-category]
- Muscular dystrophy [ICD-11 Category]
- Muscular dystrophy [MedDRA Preferred Term]
- Muscular dystrophy [ICD-10 Sub-category (who)]
- Muscular dystrophy (disorder) [SNOMED CT concept]
- muscular dystrophies [MeSH concept]
- muscular dystrophies [MeSH Descriptor]
- muscular dystrophy [DO Concept]
- muscular dystrophy [MedlinePlus Topic]
- muscular dystrophy [Artificial nutrition thesaurus concept]
- muscular dystrophy, nos [SNOMED Notion]