Phenotype #0000057848

Individual ID 00078073
Associated disease STGD1
Phenotype details Stargardt disease, severe; y47, visual acuity OD: 20/400, OS: 20/400. y44: Severe maculopathy with fleck-like chorioretinal atrophy up to far periphery. Severe cone-rod dystrophy.
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset unknown
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +01:00 (CET)
Date last edited N/A

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