Phenotype #0000210622

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00276064
Associated disease	neuropathy, optic
Phenotype details	Optic atrophy (HP:0000648)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal dominant
Age/Examination	21y (21 years)
Age/Diagnosis	-
Age/Onset	09y
Phenotype/Onset	Blurred vision (HP:0000622)
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-01-24 14:22:06 +01:00 (CET)
Date last edited	2020-08-25 21:27:59 +02:00 (CEST)

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