myopathy, congenital, Compton-North

Preferred Label : myopathy, congenital, Compton-North;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0567561;

UMLS CUI

C2675527;

Currated CISMeF NLP mapping
- Compton-North congenital myopathy [DO Concept]
- Congenital lethal myopathy Compton North type (disorder) [SNOMED CT concept]
- Congenital lethal myopathy, Compton-North type [ORDO Disease]
- Congenital myopathy 12 [OMIM Phenotype]
Related record
- myopathy, congenital, Compton-North [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Compton-North congenital myopathy [DO Concept]
- Congenital lethal myopathy, Compton-North type [ORDO Disease]
- Congenital myopathy 12 [OMIM Phenotype]