Deafness, Autosomal Recessive 31 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Deafness, Autosomal Recessive 31
Unique ID: C564629
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564629
Entry Term(s): DFNB31; Whirler, Mouse, Homolog Of
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 3
Note: mutation in WHRN
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Deafness, Autosomal Recessive 31 Preferred

page delivered in 0.003s