GUCA1B

guanylate cyclase activator 1B
OMIM: 602275
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 6.16
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Macular Dystrophy/Degeneration/Stargardt Disease, Eye Disorders, Retinitis Pigmentosa, Dominant, Retinitis pigmentosa, Retinitis pigmentosa 48, 613827