RP2

RP2, ARL3 GTPase activating protein
OMIM: 300757
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 7.0
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Retinitis pigmentosa 2, RP2-related X-linked Retinitis Pigmentosa, Eye Disorders, Retinitis pigmentosa, Retinitis pigmentosa 2, 312600, Retinitis Pigmentosa, X-linked