retinitis pigmentosa

Summary
Synonym
  • pericentral pigmentary retinopathy
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.
Super Class
retinal degeneration
Disease Ontology
DOID:10584
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 24 of 24 in total
Gene ID Gene Symbol Description Source
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
57545 CC2D2A coiled-coil and C2 domain containing 2A
80201 HKDC1 hexokinase domain containing 1
83552 MFRP membrane frizzled-related protein
Displaying all 3 entries
Gene ID Gene Symbol Description Source
21366 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6
241324 Crb2 crumbs family member 2
320234 Ccdc66 coiled-coil domain containing 66
Displaying 1 entry
Gene ID Gene Symbol Description Source
25022 Fgfr2 fibroblast growth factor receptor 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
42367 ninaE neither inactivation nor afterpotential E
42896 crb crumbs
Displaying all 2 entries
Gene ID Gene Symbol Description Source
30295 rho rhodopsin
557044 eys eyes shut homolog
Related Glycoprotein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 8, 2025