Phenotype #0000293115

Individual ID 00400074
Associated disease FVH2
Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), strabismus (HP:0000486) and nystagmus (HP:0000639)
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 InternationalCreative Commons License
Created by Mohammed A.M Derar
Date created 2022-01-24 12:50:37 +01:00 (CET)
Date last edited 2022-01-28 12:49:05 +01:00 (CET)

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