Doyne honeycomb retinal dystrophy

Summary
Synonym
  • DHRD
  • Doyne honeycomb degeneration of retina
Definition
A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium in the posterior pole of the eye in a honeycomb pattern and that has_material_basis_in mutations in the EFEMP1 gene on chromosome 2p16.
Super Class
autosomal dominant disease retinal drusen
External Links
Disease Ontology
DOID:0060745
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6120 RPE ribulose-5-phosphate-3-epimerase
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q96AT9 Ribulose-phosphate 3-epimerase

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024