Disease #07273 (DEE87 (encephalopathy, developmental and epileptic, type 87), OMIM:618916)

Official abbreviation DEE87
Name encephalopathy, developmental and epileptic, type 87
OMIM ID 618916
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CDK19
Associated tissues -
Disease features -
Remarks -
Date created 2026-07-20 13:45:18 +02:00 (CEST)
Date last edited N/A

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