Disease #03959 (DEE17;EIEE17 (developmental and epileptic encephalopathy, type 17), OMIM:615473)

Official abbreviation DEE17;EIEE17
Name developmental and epileptic encephalopathy, type 17
OMIM ID 615473
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GNAO1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-07-07 11:03:05 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00033856 - PubMed: Saitsu 2016 - F no Japan Japanese - - - - DEE17;EIEE17 movement disorder; no structural changes brain; severe developmental delay; no speech GNAO1 GNAO1 1 1 Hirotomo Saitsu
00033857 - PubMed: Saitsu 2016 - F no Japan Japanese - - - - DEE17;EIEE17 4y-onset movement disorder; 10y-11y-onset epilepsy; structural changes brain, atrophy, thinned corpus callosum; severe developmental delay; affected speech GNAO1 GNAO1 1 1 Hirotomo Saitsu
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