Global Variome shared LOVD

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

Phenotype #0000057854 Individual ID 00078079 Associated disease STGD1 Phenotype details Stargardt disease, moderate/severe; y40, visual acuity OD: 20/200, OS: 20/400. y39: Severe macular atrophy with flecks up to the mid periphery. Mild cone-rod dystrophy. Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 18y Phenotype/Onset unknown Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2016-02-22 12:22:09 +01:00 (CET) Date last edited N/A

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