Global Variome shared LOVD

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

Phenotype #0000027143 Individual ID 00033714 Associated disease STGD Phenotype details Stargardt disease; bilateral impairment of central vision together with irregular hyperfluorescent lesions at the macula and a darkchoroid Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 20y Phenotype/Onset visual deterioration, observed by patient Protein - Owner name Monika Oldak Database submission license No license selected Created by Monika Oldak Date created 2015-02-23 22:16:21 +01:00 (CET) Date last edited 2016-06-26 21:03:22 +02:00 (CEST)

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