Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000260838 Individual ID 00365500 Associated disease - Phenotype details At the age of 53, the BCVA was : HM OD and HM OS. Ultrawidefield fundus autofluorescence type was: Central atrophy and significant extramacular flecks and atrophy extending outside posterior pole. subtype: severe atrophy extending from macula to 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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.