Disease #07000 (DEE101 (encephalopathy, developmental and epileptic, type 101), OMIM:619814)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE101
Name	encephalopathy, developmental and epileptic, type 101
OMIM ID	619814
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRIN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-02-01 18:30:02 +01:00 (CET)
Date last edited	N/A

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