facioscapulohumeral muscular dystrophy 1B

Preferred Label : facioscapulohumeral muscular dystrophy 1B;

MeSH synonym : FSHMD1B; muscular dystrophy, facioscapulohumeral, type 1B; FSHD1B;

Details

Origin ID

C563557;

UMLS CUI

C1834671;

Currated CISMeF NLP mapping
- Facioscapulohumeral Muscular Dystrophy 2 [NCIt concept]
- Facioscapulohumeral muscular dystrophy 2, digenic [OMIM Phenotype]
- facioscapulohumeral muscular dystrophy 2 [DO Concept]
MeSH term(s) associated for indexing
- muscular dystrophy, facioscapulohumeral [MeSH Descriptor]
Record concept(s)
- facioscapulohumeral muscular dystrophy 1B [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Facioscapulohumeral Muscular Dystrophy 2 [NCIt concept]
- Facioscapulohumeral muscular dystrophy 2, digenic [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients