Phenotype #0000222594

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00288898
Associated disease	neuropathy, optic
Phenotype details	Amblyopia (HP:0000646)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal dominant
Age/Examination	09y (9 years)
Age/Diagnosis	-
Age/Onset	04y
Phenotype/Onset	-
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-02-24 21:09:40 +01:00 (CET)
Date last edited	2020-08-25 21:27:59 +02:00 (CEST)

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