Global Variome shared LOVD

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Phenotype #0000298473 Individual ID 00405975 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), Posterior embryotoxon (HP:0000627) & goniodysgenesis. Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal Hypoplasia 2 Age/Examination 03y (3 years) 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 2022-03-24 13:41:18 +01:00 (CET) Date last edited N/A

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