|
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 - skin of anterior chest |
| 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)