Disease #07120 (DEE31B (developmental and epileptic encephalopathy, type 31B), OMIM:602377)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE31B
Name	developmental and epileptic encephalopathy, type 31B
OMIM ID	602377
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNM1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-11 21:52:37 +01:00 (CET)
Date last edited	N/A

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