Global Variome shared LOVD

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Phenotype #0000292518 Individual ID 00399407 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639), Hypopigmentation of the fundus (HP:0007894), Posterior embryotoxon (HP:0000627), Reduced visual acuity (HP:0007663) and Optic nerve misrouting (HP:0025551) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal hypoplasia 2 Age/Examination - Age/Diagnosis 74y 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 2022-01-20 15:54:10 +01:00 (CET) Date last edited 2022-01-24 12:22:14 +01:00 (CET)

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