Global Variome shared LOVD

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

Phenotype #0000264665 Individual ID 00369327 Associated disease - Phenotype details The BCVA (logMAR) RE/LE, was 48y: 1,0/1,0 50y: 1,0/1,0 60y: 1,3/1,3, the VF RE/LE (RE/LE VFI %) was NA. The Fundus examination was 50y: macular RPE atrophy, yellow flecks around the macula.. The FAF was NA. The OCT was 50y: central and periph NE thinning. and the Vision electrophysiology was NA. Additional findings were: Myopia, 60y: BE SCP catar. Diagnosis/Initial Stargardt disease Inheritance Unknown Diagnosis/Definite STGD1 Age/Examination - Age/Diagnosis - Age/Onset 40y Phenotype/Onset Childhood: photo, NB, decr VA. 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.