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Summary Literature (14)
DOID:10584 - retinitis pigmentosa

Disease Ontology 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.

Synonyms: pericentral pigmentary retinopathy

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : crx, crb1, nr2e3, prpf31, mak, mertk, prpf4, fscn2, prom1, aipl1, arl6, arl2bp, rp9, pde6g, cnga1, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): retinal degeneration (is_a)

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Version: 4.14.0
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