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XB-GENEPAGE-983509
pitpnm3 PITPNM family member 3
Monarch Ortholog Phenotypes
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Human (9 sources): Abnormality of retinal pigmentation, Color vision defect, Cone dystrophy, Cone/cone-rod dystrophy, Macular degeneration, Nyctalopia, Photophobia, Reduced visual acuity, Visual impairment |
View all ortholog results at Monarch |