congenital hereditary muscular dystrophy

Preferred Label : congenital hereditary muscular dystrophy;

Origin ID

DA-51110;

UMLS CUI

C2937300;

Currated CISMeF NLP mapping
- Becker muscular dystrophy [DO Concept]
- Becker muscular dystrophy [PASCAL descriptor]
- Becker muscular dystrophy [Disease (Nov.)]
- Becker's Muscular Dystrophy [NCIt concept]
- Becker's muscular dystrophy [MedDRA Preferred Term]
- Benign congenital myopathy (disorder) [SNOMED CT concept]
- Congenital hereditary muscular dystrophy [ICD-9 code]
- Congenital hereditary muscular dystrophy (disorder) [SNOMED CT concept]
- Muscular dystrophy, becker type [OMIM Phenotype]
- becker muscular dystrophy [MeSH concept]
ICD-10 exact mapping(s)
- Congenital myopathies [ICD-10 Sub-category (who)]
Metaterm(s)
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Congenital hereditary muscular dystrophy (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- Becker muscular dystrophy [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital hereditary muscular dystrophy [ICD-9 code]
- Congenital hereditary muscular dystrophy (disorder) [SNOMED CT concept]
- congenital muscular dystrophy [DO Concept]