myopathies, nemaline

Preferred Label : myopathies, nemaline;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0026760;

UMLS CUI

C0206157;

Currated CISMeF NLP mapping
- Hereditary disorder of musculoskeletal system (disorder) [SNOMED CT concept]
- Nemaline myopathy [PASCAL descriptor]
- Nemaline myopathy [Disease (Nov.)]
- Nemaline myopathy [ICD-11 Sub-sub category]
- Nemaline myopathy [ORDO Disease]
- Nemaline myopathy (disorder) [SNOMED CT concept]
- nemaline myopathy [DO Concept]
- nemaline myopathy [SNOMED Notion]
MeSH narrower concept(s)
- adult onset nemaline myopathy [MeSH concept]
- nemaline myopathy, autosomal dominant [MeSH concept]
- nemaline myopathy, autosomal recessive [MeSH concept]
- nemaline myopathy, childhood onset [MeSH concept]
- nemaline myopathy, late onset [MeSH concept]
Related record
- myopathies, nemaline [MeSH Descriptor]
See also inter- (CISMeF)
- Centronuclear myopathy [ICD-11 Sub-sub category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nemaline myopathy [ORDO Disease]
- Nemaline myopathy [PASCAL descriptor]
- Nemaline myopathy [Disease (Nov.)]
- Nemaline myopathy [ICD-11 Sub-sub category]
- Nemaline myopathy (disorder) [SNOMED CT concept]
- nemaline myopathy [SNOMED Notion]
- nemaline myopathy [DO Concept]