Global Variome shared LOVD

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Phenotype #0000294424 Individual ID 00401650 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal Hypoplasia Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mohammed A.M Derar Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Mohammed A.M Derar Date created 2022-02-01 14:00:02 +01:00 (CET) Date last edited N/A

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