Global Variome shared LOVD

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

Phenotype #0000174269 Individual ID 00233846 Associated disease STGD Phenotype details visual acuity now R-counting vingers L-counting vingers; mild central vision defect; ERG rod-normal/cone-normal Diagnosis/Initial Stargardt disease Inheritance Familial, autosomal recessive Diagnosis/Definite STGD-1 Age/Examination 63y (63 years) Age/Diagnosis 23y Age/Onset - Phenotype/Onset - Protein - Owner name Terry-Lynn Young Database submission license No license selected Created by Jim Houston Date created 2019-03-20 11:55:21 +01:00 (CET) Date last edited N/A

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