Deafness, Autosomal Dominant 11 MeSH Supplementary Concept Data 2025

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 Numbers: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 4
Note: mutation in MYO7A
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Deafness, Autosomal Dominant 11 Preferred

page delivered in 0.002s