deafness, autosomal dominant, due to mutation in Myo1a - CISMeF

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CISMeF

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Deafness, autosomal dominant, due to mutation in Myo1aMeSH Supplementary Concept

Preferred Label : deafness, autosomal dominant, due to mutation in Myo1a;

Details

Origin ID

C567266;

UMLS CUI

C3502294;

MeSH term(s) associated for indexing
- hearing loss [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant, due to mutation in Myo1a [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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10/06/2024

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