Disease #02197 (EIEE36;CDG1S (epileptic encephalopathy, early infantile, 36), OMIM:300884)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EIEE36;CDG1S
Name	epileptic encephalopathy, early infantile, 36
OMIM ID	300884
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALG13
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 22:02:57 +01:00 (CET)

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