cone dystrophy

Summary
Synonym
  • retinal cone dystrophy
Definition
A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.
Super Class
retinal disease
External Links
Disease Ontology
DOID:0050795
Mondo Disease Ontology
MeSH
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
93589 CACNA2D4 calcium voltage-gated channel auxiliary subunit alpha2delta 4
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q7Z3S7 Voltage-dependent calcium channel subunit alpha-2/delta-4

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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: August 19, 2024