Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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:
OMIM:268000 - RETINITIS PIGMENTOSA; RP

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)


Xenbase: The Xenopus Model Organism Knowledgebase.
Version: 4.14.0
Major funding for Xenbase is provided by grant P41 HD064556