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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,
Echinobase Genes : prpf31, prom1, idh3b, snrnp200, slc7a14, prpf8, rp2, rpgr, dhdds, arl6, prpf4, prpf6, arl2bp, c8orf37, nr2e3
MIM:268000 - retinitis pigmentosa; rp |
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)