Phenotype #0000222977

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00289359
Associated disease	CCM1
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	Cavernous malformation of the optic nerve
Inheritance	Familial, autosomal dominant
Age/Examination	30y (30 years)
Age/Diagnosis	30y
Age/Onset	30y
Phenotype/Onset	-
Protein	-
Owner name	Stefania Battistini
Database submission license	No license selected
Created by	Stefania Battistini
Date created	2020-03-05 11:36:31 +01:00 (CET)
Date last edited	2020-04-02 19:55:12 +02:00 (CEST)

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