Phenotype #0000171799

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00227777
Associated disease	?
Diagnosis/Initial	Neonatal epilepsy
Diagnosis/Definite	-
Phenotype details	hypotonia, developmental delay and regression, ataxia, and autistic features
Inheritance	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	LOVD
Database submission license	No license selected
Created by	Hirotomo Saitsu
Date created	2011-09-04 05:05:51 +02:00 (CEST)
Date last edited	N/A

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