Phenotype #0000078638

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00100436
Associated disease	EIEE
Phenotype details	severe early infantile encephalopathy (global) hyperkinetic stereotypic movements "oculogyric like" eye movements
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	02y (2 years)
Age/Diagnosis	-
Age/Onset	00y02m
Phenotype/Onset	-
Protein	-
Intellectual_dis	profound
Owner name	Ronen Spiegel
Database submission license	No license selected
Created by	Ronen Spiegel
Date created	2017-02-23 22:46:32 +01:00 (CET)
Date last edited	2017-03-05 16:23:41 +01:00 (CET)

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