Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8 [Supplementary Concept]

mutation in TMPRSS3

Date introduced: November 5, 2012

MeSH Unique ID: C563395

Heading Mapped to:

• Hearing Loss, Sensorineural

Entry Terms:

• Neurosensory Nonsyndromic Recessive Deafness 8