RP1

RP1, axonemal microtubule associated
OMIM: 603937
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Retinitis pigmentosa 1, Eye Disorders, Retinitis pigmentosa 1, 180100{Hypertriglyceridemia, susceptibility to}, 145750, Retinitis Pigmentosa, Dominant, Retinitis pigmentosa, rod-cone dystrophy