Global Variome shared LOVD

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

Phenotype #0000317826 Individual ID 00426671 Associated disease - Phenotype details VA: 20/80(RE) - 20/80(LE); Foveal pigment disruption with flecks Diagnosis/Initial Stargardt disease (adSTGD-like) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 33y (33 years) Age/Diagnosis - Age/Onset 27y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-12-02 14:17:29 +01:00 (CET) Date last edited N/A

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