Phenotype #0000129932

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	00165061
Associated disease	CCM
Phenotype details	-
Diagnosis/Initial	cerebral cavernous malformations
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CCM-1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Carmela Fusco
Database submission license	No license selected
Created by	Carmela Fusco
Date created	2018-06-21 10:40:15 +02:00 (CEST)
Date last edited	N/A

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