myopathy, X-Linked, with excessive autophagy

Preferred Label : myopathy, X-Linked, with excessive autophagy;

Origin ID

C564093;

UMLS CUI

C1839615;

Automatic exact mappings (from CISMeF team)
- X-linked myopathy with excess autophagy [ICD-11 More detail]
Currated CISMeF NLP mapping
- Myopathy, X-linked, with excessive autophagy [OMIM Phenotype]
- X-linked myopathy with excessive autophagy [DO Concept]
- X-linked myopathy with excessive autophagy [ORDO Disease]
- X-linked myopathy with excessive autophagy (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- muscular diseases [MeSH Descriptor]
Record concept(s)
- myopathy, X-Linked, with excessive autophagy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myopathy, X-linked, with excessive autophagy [OMIM Phenotype]
- X-linked myopathy with excessive autophagy [DO Concept]
- X-linked myopathy with excessive autophagy (disorder) [SNOMED CT concept]