Phenotype #0000027252

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00033854
Associated disease	EEOC
Phenotype details	movement disorder; developmental epileptic encephalopathy; 2m-onset epilepsy; structural changes brain, atrophy, thinned corpus callosum; severe developmental delay; no speech
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	00y02m
Phenotype/Onset	-
Protein	-
Owner name	Hirotomo Saitsu
Database submission license	No license selected
Created by	Hirotomo Saitsu
Date created	2015-03-07 04:04:28 +01:00 (CET)
Date last edited	2023-10-19 15:18:47 +02:00 (CEST)

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