scleroatonic muscular dystrophy

Preferred Label : scleroatonic muscular dystrophy;

MeSH synonym : ullrich disease; late onset scleroatonic familial myopathy; ullrich congenital muscular dystrophy; ullrich scleroatonic muscular dystrophy; muscular dystrophy, scleroatonic; Ullrich congenital muscular dystrophy 1;

Details

Origin ID

C537521;

UMLS CUI

C0410179;

Automatic exact mappings (from CISMeF team)
- Ullrich congenital muscular dystrophy [ICD-11 More detail]
- Ullrich congenital muscular dystrophy [OMIM phenotypic series]
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 1 [OMIM Phenotype]
- congenital hypotonic sclerotic muscular dystrophy [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophies [MeSH Descriptor]
- sclerosis [MeSH Descriptor]
Record concept(s)
- Scleroatonic muscular dystrophy [MeSH 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 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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