MERTK

MER proto-oncogene, tyrosine kinase
OMIM: 604705
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Retinitis pigmentosa 38, childhood onset rod-cone dystrophy with early macular atrophy, Leber congenital amaurosis, Retinitis pigmentosa 38, Eye Disorders, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive, Retinitis pigmentosa 38, 613862