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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 (3)

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)
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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory