Global Variome shared LOVD

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Phenotype #0000300839 Individual ID 00408720 Associated disease - Phenotype details 60y, had night blindness and macular degeneration for decade; rod sensitivity loss - about one log unit in the peripheral field; extensive central scotoma; no improvement after vitamin A supplementation Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite Sorsby fundus dystrophy Age/Examination 60y (60 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-04-26 11:12:04 +02:00 (CEST) Date last edited N/A

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