Version: 8.0.0Date: Tue Jan 28 2025
Disease Genes: PRPF3 (Hsa)
Disease
Source: DOID:10584
Definition: A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss.
Genes: PRPF3 (Hsa)
Disease
Source: DOID:0110356
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the PRPF3 gene on chromosome 1q21.
Genes: PRPF3 (Hsa)