Deafness, Autosomal Dominant 48 MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Deafness, Autosomal Dominant 48
Unique ID: C564322
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564322
Entry Term(s): DFNA48
Registry Number: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 1
Note: mutation in MYO1A
Date of Entry: 2012/11/05

Deafness, Autosomal Dominant 48 Preferred

page delivered in 0.004s