Phenotype #0000078872

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	00100621
Associated disease	CM1
Phenotype details	-
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	08y (8 years)
Age/Onset	08y
Phenotype/Onset	scaphocephaly, Chiari malformation type I
Protein	-
Owner name	Patrizia De Marco
Database submission license	No license selected
Created by	Patrizia De Marco
Date created	2017-03-07 15:10:46 +01:00 (CET)
Date last edited	2017-03-07 17:06:43 +01:00 (CET)

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