minicore myopathy, moderate, with hand involvement

Preferred Label : minicore myopathy, moderate, with hand involvement;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566447;

UMLS CUI

C1861751;

Automatic exact mappings (from CISMeF team)
- Congenital myopathy 1a, autosomal dominant, with susceptibility to malignant hyperthermia [OMIM Phenotype]
- Moderate multiminicore disease with hand involvement [ORDO Disease]
Related MeSH concept(s)
- multicore myopathy, moderate, with hand involvement [MeSH concept]
- multiminicore disease, moderate, with hand involvement [MeSH concept]
Related record
- minicore myopathy, moderate, with hand involvement [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Moderate multi-minicore disease with hand involvement [ICD-11 More detail]