Phenotype #0000157635

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00209029
Associated disease	RD
Phenotype details	Retinal dystrophy
Diagnosis/Initial	retinal dystrophy
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	STGD-1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-12-22 15:10:51 +01:00 (CET)
Date last edited	N/A

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