Scleroatonic muscular dystrophy

Preferred Label : Scleroatonic muscular dystrophy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531982;

UMLS CUI

C0410179;

Automatic exact mappings (from CISMeF team)
- Ullrich congenital muscular dystrophy [ICD-11 More detail]
Currated CISMeF NLP mapping
- Congenital muscular dystrophy, Ullrich type [ORDO Disease]
- Ullrich Congenital Muscular Dystrophy [NCIt concept]
- Ullrich congenital muscular dystrophy [PASCAL descriptor]
- Ullrich congenital muscular dystrophy [DO Concept]
- Ullrich congenital muscular dystrophy (disorder) [SNOMED CT concept]
- Ullrich congenital muscular dystrophy 1a [OMIM Phenotype]
- congenital hypotonic sclerotic muscular dystrophy [Disease (Nov.)]
Related record
- scleroatonic muscular dystrophy [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital muscular dystrophy, Ullrich type [ORDO Disease]
- Ullrich Congenital Muscular Dystrophy [NCIt concept]
- Ullrich congenital muscular dystrophy 1a [OMIM Phenotype]