SLITRK6

SLIT and NTRK like family member 6
OMIM: 609681, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green SLITRK6 in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Deafness and myopia, OMIM:221200
    • high myopia-sensorineural deafness syndrome MONDO:0009082