Phenotype #0000310973

Individual ID 00419693
Associated disease -
Phenotype details -
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Rebekkah Hitti-Malin
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-10-21 12:50:15 +02:00 (CEST)
Date last edited N/A

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