Phenotype #0000056331

Individual ID 00076556
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Stargardt disease or cone-rod dystrophy or retinits pigmentosa; Of the patients, 67,7% had Stargardt disease, 27,7% Cone-rod dystrophy, 4,6% had retinitis pigmentosa.
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset unknown
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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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