Global Variome shared LOVD

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Phenotype #0000056958 Individual ID 00077183 Associated disease STGD1 Phenotype details Stargardt disease, late onset; y64: Visual actuity: OD 20/15, OS 20/15, Flavimaculatus flecks with foveal sparing, dark choroid. Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 61y Phenotype/Onset The onset of STGD1 was defined as the age at initial symptoms. In asymptomatic cases, we used the age at first diagnosis, defined as the age at which macular abnormalities were diagnosed for the first time by an ophthalmologist 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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