becker generalized myotonia

Preferred Label : becker generalized myotonia;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0540216;

UMLS CUI

C0751360;

Automatic exact mappings (from CISMeF team)
- Becker muscular dystrophy (disorder) [SNOMED CT concept]
- Myotonia congenita, autosomal recessive [OMIM Phenotype]
Related record
- myotonia congenita [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital myotonia, autosomal recessive form (disorder) [SNOMED CT concept]
- Myotonia congenita, autosomal recessive [OMIM Phenotype]
- congenital myotonia, autosomal recessive form [SNOMED Notion]