Deafness, Autosomal Dominant 11 MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Deafness, Autosomal Dominant 11
Unique ID: C563353
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563353
Entry Term(s): DFNA11
Registry Number: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 4
Note: mutation in MYO7A
Date of Entry: 2012/11/05

Deafness, Autosomal Dominant 11 Preferred

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