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Summary Literature (0)
DOID:0060746 - basal laminar drusen

Disease Ontology Definition:A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has_material_basis_in mutations in the CFH gene on chromosome 1q31.3.

Synonyms: cuticular drusen, drusen of bruch membrane, early adult-onset grouped drusen

Xenbase Genes : cfh

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007472 - basal laminar drusen


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): monogenic disease (is_a), retinal drusen (is_a)