SLITRK6

SLIT and NTRK like family member 6
OMIM: 609681
PanelMode of inheritanceDetails
1 panel
R-numbers: R67
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Deafness and myopia, OMIM:221200, high myopia-sensorineural deafness syndrome MONDO:0009082