macular degeneration age-related macular degeneration familial flecked retinopathy Stargardt disease https://rarediseases.info.nih.gov/diseases/181/stargardt-disease fundus flavimaculatus UMLS:C0271093 Stargardt disease 1 MESH:D000080362 juvenile onset macular degeneration Stargardt 1 NCIT:C85078 MONDO:0019353 Stargardt macular dystrophy Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion. GARD:0000181 icd11.foundation:1690038580 SCTID:47673003 DOID:0050817 Orphanet:827 OMIMPS:248200 NANDO:1200933 MedDRA:10062766 MEDGEN:75734