myopathy, reducing body, X-Linked, Childhood-Onset - CISMeF

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CISMeF

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Myopathy, reducing body, X-Linked, Childhood-OnsetMeSH Supplementary Concept

Preferred Label : myopathy, reducing body, X-Linked, Childhood-Onset;

MeSH note : mutations in FHL1;

Details

Origin ID

C567468;

UMLS CUI

C2678015;

Currated CISMeF NLP mapping
- Reducing body myopathy, X-linked 1b, with late childhood or adult onset [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- muscular diseases [MeSH Descriptor]
Record concept(s)
- myopathy, reducing body, X-Linked, Childhood-Onset [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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19/05/2024

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