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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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
retinal degeneration (is_a)