Disease #07189 (DEE111 (encephalopathy, developmental and epileptic, type 111), OMIM:620504)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE111
Name	encephalopathy, developmental and epileptic, type 111
OMIM ID	620504
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DEPDC5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-09-30 18:15:03 +02:00 (CEST)
Date last edited	N/A

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