Phenotype #0000292623

Individual ID 00399518
Associated disease FVH2
Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), posterior embryotoxon (HP:0000627) and cataracts (HP:0000518)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite Foveal Hypoplasia 2
Age/Examination -
Age/Diagnosis 39y
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 12:56:41 +01:00 (CET)
Date last edited 2022-01-28 15:32:28 +01:00 (CET)

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