Disease #04668 (DEE117;CMS18 (encephalopathy, developmental and epileptic, type 117), OMIM:616330)

Official abbreviation DEE117;CMS18
Name encephalopathy, developmental and epileptic, type 117
OMIM ID 616330
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 SNAP25
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2025-09-30 18:07:24 +02:00 (CEST)


Individuals

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00474012 364950 - - M no Germany - - - - - DEE117;CMS18 Intellectual disability, EEG abnormality SNAP25 SNAP25 1 1 Andreas Laner
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