MeSH Browser

MeSH Supplementary: Deafness, Autosomal Recessive 9
Unique ID: C563396
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563396
Entry Term(s): Auditory Neuropathy, Autosomal Recessive, 1; Neurosensory Nonsyndromic Recessive Deafness 9
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 2
Note: mutationin otoferlin
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Deafness, Autosomal Recessive 9 MeSH Supplementary Concept Data 2024