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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
Xenbase Genes : crx, cdhr1, crb1, nr2e3, ift88, prpf31, mak, mertk, prpf4, fscn2, prom1, aipl1, bbs2, arl6, spata7,
MONDO:0019200 - retinitis pigmentosa |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
retinal degeneration (is_a)