Genomics England
GMS Panels
Panels
Genes and Entities

SLITRK6

SLIT and NTRK like family member 6
OMIM: 609681
PanelMode of inheritanceDetails
1 panel
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.23
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Deafness and myopia, OMIM:221200, high myopia-sensorineural deafness syndrome MONDO:0009082