Phenotype #0000292498

Individual ID 00399387
Associated disease FVH2
Phenotype details Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), astigmatism (HP:0000483) and moderate hypermetropia (HP:0031729)
Diagnosis/Initial Albinism
Inheritance Familial, autosomal recessive
Diagnosis/Definite Foveal Hypoplasia
Age/Examination -
Age/Diagnosis 32y
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 2022-01-20 13:24:00 +01:00 (CET)
Date last edited 2022-01-24 12:15:35 +01:00 (CET)

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