Global Variome shared LOVD

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Phenotype #0000292492 Individual ID 00399380 Associated disease FVH2 Phenotype details ypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), posterior embryotoxon (HP:0000627) and Hypopigmentation of the fundus (HP:0007894) Diagnosis/Initial ocular albinism Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal hypoplasia 2 Age/Examination - Age/Diagnosis 14y 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 12:51:12 +01:00 (CET) Date last edited 2022-01-24 12:12:54 +01:00 (CET)

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