Global Variome shared LOVD

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Phenotype #0000303735 Individual ID 00411708 Associated disease - Phenotype details BCVA was 0.2 in OU, red?green defect and central relative scotoma in OU Diagnosis/Initial occult macular dystrophy (OMD) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 38y (38 years) Age/Diagnosis - Age/Onset 15y Phenotype/Onset progressive visual decline, associated with photophobia Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-06-18 03:05:08 +02:00 (CEST) Date last edited N/A

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