Global Variome shared LOVD

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Phenotype #0000292646 Individual ID 00399541 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750), Nystagmus (HP:0000639), Reduced visual acuity (HP:0007663) and strabismus (HP:0000486). Diagnosis/Initial infantile nystagmus and foveal hypoplasia Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal Hypoplasia 2 Age/Examination - Age/Diagnosis 03y 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 2022-01-21 15:59:11 +01:00 (CET) Date last edited 2022-01-28 12:30:12 +01:00 (CET)

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