Disease #03961 (DEE18 (encephalopathy, developmental and epileptic, type 18), OMIM:615476)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE18
Name	encephalopathy, developmental and epileptic, type 18
OMIM ID	615476
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SZT2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-12-30 12:37:26 +01:00 (CET)

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