Disease #07049 (DEE89 (encephalopathy, developmental and epileptic, type 89), OMIM:619124)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE89
Name	encephalopathy, developmental and epileptic, type 89
OMIM ID	619124
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GAD1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-12-04 21:51:10 +01:00 (CET)
Date last edited	N/A

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