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 InternationalCreative Commons License
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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