Phenotype #0000056825

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00077050
Associated disease	?
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	cohort of 73% Stargardt disease, 16% Retinitis pigmentosa, 11% macular dystrophy
Inheritance	Unknown
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	unknown
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Stéphanie Cornelis
Database submission 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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