congenital myotonia, autosomal recessive form

Preferred Label : congenital myotonia, autosomal recessive form;

Origin ID

DA-51324;

UMLS CUI

C0751360;

Currated CISMeF NLP mapping
- Congenital myotonia, autosomal recessive form (disorder) [SNOMED CT concept]
- Myotonia congenita, recessive [ICD-11 More detail]
ICD-10 exact mapping(s)
- Myotonic disorders [ICD-10 Sub-category (who)]
Metaterm(s)
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Congenital myotonia, autosomal recessive form (disorder) [SNOMED CT concept]
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]
- becker generalized myotonia [MeSH concept]