Disease #04495 (DEE27 (encephalopathy, developmental and epileptic, type 27), OMIM:616139)

Official abbreviation DEE27
Name encephalopathy, developmental and epileptic, type 27
OMIM ID 616139
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GRIN2B
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2023-02-01 18:27:50 +01:00 (CET)


Individuals

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00437992 48747 - - M no Germany - - - - - DEE27 Intellectual disability, mild, Seizure, Atypical behavior, Abnormal aggressive, impulsive or violent behavior GRIN2B GRIN2B 1 1 Andreas Laner
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