Disease #03961 (DEE18 (encephalopathy, developmental and epileptic, type 18), OMIM:615476)

Official abbreviation DEE18
Name encephalopathy, developmental and epileptic, type 18
OMIM ID 615476
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SZT2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-12-30 12:37:26 +01:00 (CET)


Individuals

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00380781 ? PubMed: Nair 2018 - ? - Lebanon - - - - - DEE18 DD; Seizures (Neurological) - SZT2 1 1 LOVD
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