Phenotype #0000242872

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00324329
Associated disease	CORD5
Phenotype details	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608
Diagnosis/Initial	cone-rod dystrophy
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CORD5
Age/Examination	08y (8 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Mariah De Bruin
Database submission license	No license selected
Created by	Mariah De Bruin
Date created	2020-12-07 11:39:53 +01:00 (CET)
Date last edited	2020-12-11 10:05:39 +01:00 (CET)

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