facioscapulohumeral muscular dystrophy 1a

Preferred Label : facioscapulohumeral muscular dystrophy 1a;

MeSH note : PROM;

MeSH synonym : facioscapulohumeral muscular dystrophy, infantile; muscular dystrophy, facioscapulohumeral, type 1a; FSHMD1A; landouzy-dejerine muscular dystrophy; facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles; FSHD1A;

Details

Origin ID

C536391;

UMLS CUI

C1834673;

Automatic exact mappings (from CISMeF team)
- Facioscapulohumeral muscular dystrophy (disorder) [SNOMED CT concept]
- Facioscapulohumeral muscular dystrophy 1 [OMIM Phenotype]
- facioscapulohumeral muscular dystrophy [DO Concept]
- facioscapulohumeral muscular dystrophy 1 [DO Concept]
MeSH term(s) associated for indexing
- muscular dystrophy, facioscapulohumeral [MeSH Descriptor]
Record concept(s)
- Facioscapulohumeral muscular dystrophy 1a [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Facioscapulohumeral muscular dystrophy 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients