Phenotype #0000293126

Individual ID 00400085
Associated disease FVH2
Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663) and nystagmus (HP:0000639).
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite Foveal Hypoplasia 2
Age/Examination -
Age/Diagnosis 02y
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 2022-01-24 14:28:39 +01:00 (CET)
Date last edited 2022-01-28 12:43:38 +01:00 (CET)

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