Global Variome shared LOVD

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

Phenotype #0000057558 Individual ID 00077783 Associated disease STGD1 Phenotype details Stargardt disease; y44: Visual acuity OD -0.1 logMAR, OS -0.1 logMAR, multiple patchy atrophic lesions, extending beyond the arcades, PERG P50 abnormality and additional generalized cone and rod system abnormality. Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 39y Phenotype/Onset visual loss or the latest examination for asymptomatic patients. 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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