Phenotype #0000155673

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	00207889
Associated disease	?
Diagnosis/Initial	-
Diagnosis/Definite	MRD-19
Phenotype details	Global developmental delay; spasticity; microcephaly
Inheritance	Familial, autosomal dominant
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-12-02 17:52:50 +01:00 (CET)
Date last edited	N/A

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