Global Variome shared LOVD

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Phenotype #0000307212 Individual ID 00415418 Associated disease - Phenotype details clinical phenotypes of 15 affected members of Family 1 (GC4059) have been previously described (Godley et al., 1996) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite progressive bifocal chorioretinal atrophy (PBCRA) Age/Examination - 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 2022-08-13 21:02:16 +02:00 (CEST) Date last edited N/A

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