Global Variome shared LOVD

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Phenotype #0000295926 Individual ID 00403183 Associated disease - Phenotype details best-corrected visual acuity right, left eye: 20/32, 20/50, pseudohypopyon/ atrophy, choroidal neovascularization left eye Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite dystrophy, macular, vitelliform type 2 (VMD2) Age/Examination 23y (23 years) Age/Diagnosis - Age/Onset 16y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-02-18 10:57:59 +01:00 (CET) Date last edited N/A

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