Term Name:	familial benign fleck retina
Synonyms:	FRFB
Definition:	A retinal disease characterized by a striking pattern of diffuse, yellow-white, fleck-like lesions extending to the far periphery of the retina but with no apparent visual or electrophysiologic deficits that has_material_basis_in homozygous or compound heterozygous mutation in the PLA2G5 gene on chromosome 1p36.13.
Ontology:	Human Disease [DOID:0111677]   ( DOID:0111677 )