Disease #05799 (EIEE63 (encephalopathy, epileptic, early infantile, type 63 (EIEE63)), OMIM:617976)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EIEE63
Name	encephalopathy, epileptic, early infantile, type 63 (EIEE63)
OMIM ID	617976
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CPLX1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-07-25 17:23:03 +02:00 (CEST)
Date last edited	N/A

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