Global Variome shared LOVD

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Phenotype #0000260832 Individual ID 00365494 Associated disease - Phenotype details At the age of 36, the BCVA was : 20/150 OD and 20/250 OS. Ultrawidefield fundus autofluorescence type was: Central atrophy and significant extramacular flecks and atrophy extending outside posterior pole. subtype: mild/moderate atrophy (most often in punctate pattern) extending to or beyond equator Diagnosis/Initial Stargardt disease Inheritance Unknown Diagnosis/Definite STGD1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset unknown Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2021-05-03 14:25:36 +02:00 (CEST) Date last edited N/A

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