severe x-linked myotubular myopathy

Preferred Label : severe x-linked myotubular myopathy;

Origin ID

DA-51528;

UMLS CUI

C0410203;

Currated CISMeF NLP mapping
- Myopathy, centronuclear, X-linked [OMIM Phenotype]
- Severe X-linked myotubular myopathy (disorder) [SNOMED CT concept]
- Severe infantile myotubular myopathy [ICD-11 More detail]
- X-Linked Centronuclear Myopathy [NCIt concept]
- X-linked centronuclear myopathy [ORDO Disease]
- x linked myotubular myopathy [Disease (Nov.)]
ICD-10 exact mapping(s)
- Congenital myopathies [ICD-10 Sub-category (who)]
Metaterm(s)
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Severe X-linked myotubular myopathy (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Myopathy, centronuclear, X-linked [OMIM Phenotype]
- Severe X-linked myotubular myopathy (disorder) [SNOMED CT concept]
- Severe infantile myotubular myopathy [ICD-11 More detail]
- X-Linked Centronuclear Myopathy [NCIt concept]
- X-linked centronuclear myopathy [ORDO Disease]
- centronuclear myopathy X-linked [DO Concept]
- x linked myotubular myopathy [Disease (Nov.)]