becker muscular dystrophy

Preferred Label : becker muscular dystrophy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0014255;

UMLS CUI

C0917713;

Currated CISMeF NLP mapping
- Becker muscular dystrophy [PASCAL descriptor]
- Becker muscular dystrophy [DO Concept]
- Becker muscular dystrophy [Disease (Nov.)]
- Becker muscular dystrophy [ICD-11 Subcategory]
- Becker muscular dystrophy [ORDO Disease]
- Becker muscular dystrophy (disorder) [SNOMED CT concept]
- Becker's Muscular Dystrophy [NCIt concept]
- Becker's muscular dystrophy [MedDRA Preferred Term]
- Benign congenital myopathy (disorder) [SNOMED CT concept]
- Muscular dystrophy, becker type [OMIM Phenotype]
- congenital hereditary muscular dystrophy [SNOMED Notion]
Related record
- muscular dystrophy, duchenne [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Becker muscular dystrophy [ORDO Disease]
- Becker muscular dystrophy [PASCAL descriptor]
- Becker muscular dystrophy [Disease (Nov.)]
- Becker muscular dystrophy (disorder) [SNOMED CT concept]
- Becker's Muscular Dystrophy [NCIt concept]
- Becker's muscular dystrophy [MedDRA Preferred Term]
- Muscular dystrophy, becker type [OMIM Phenotype]