About   Help   FAQ
Disease Ontology Browser
Doyne honeycomb retinal dystrophy (DOID:0060745)
Alliance: disease page
Synonyms: DHRD; Doyne honeycomb degeneration of retina
Alt IDs: OMIM:126600, ICD10CM:H35.5, MESH:C535602, ORDO:75376
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.

Disease References using Mouse Models (4)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory