Global Variome shared LOVD

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Phenotype #0000293114 Individual ID 00400073 Associated disease FVH2 Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639) and macrocephaly (HP:0000256) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Foveal Hypoplasia 2 Age/Examination - Age/Diagnosis 01y 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 2022-01-24 12:34:59 +01:00 (CET) Date last edited 2022-01-28 12:46:55 +01:00 (CET)

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