Deafness, Autosomal Dominant 20 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Deafness, Autosomal Dominant 20
Unique ID: C565754
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565754
Entry Term(s): DFNA20; DFNA26
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 3
Note: mutation in ACTG1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Deafness, Autosomal Dominant 20 Preferred

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