Global Variome shared LOVD

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Phenotype #0000292577 Individual ID 00399472 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750) and Reduced visual acuity (HP:0007663) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - 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 2022-01-20 20:09:14 +01:00 (CET) Date last edited 2022-01-28 15:26:40 +01:00 (CET)

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