Genomics England
GMS Panels
Panels
Genes and Entities

OTOA

otoancorin
OMIM: 607038
PanelMode of inheritanceDetails
1 panel
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hearing loss, #607039: Deafness, autosomal recessive 22 [Deafness, sensorineural, severe to profound affecting all frequencies]