has material basis in autosomal recessive disease Stargardt disease Stargardt disease 1 claudiasbj disease_ontology A stargardt disease that is characterized by juvenile-onset macular dystrophy with rapid central visual impairment, progressive bilateral atrophy of the foveal retinal pigment epithelium, and the frequent appearance of yellowish flecks, defined as lipofuscin deposits, around the macula and/or in the central and near-peripheral areas of the retina and has_material_basis_in homozygous or compound heterozygous mutation in the ABCA4 gene on chromosome 1p22. MIM:248200 DOID:0061241 autosomal recessive inheritance