Global Variome shared LOVD

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Phenotype #0000361874 Individual ID 00477264 Associated disease AN Phenotype details foveal hypoplasia Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite aniridia Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mohammed A.M Derar Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Mohammed A.M Derar Date created 2026-04-26 12:12:33 +02:00 (CEST) Date last edited 2026-04-29 09:31:31 +02:00 (CEST)

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