Disease #00156 (EPM11 (Progressive Myoclonic Epilepsy 11), OMIM:618876)

Official abbreviation EPM11
Name Progressive Myoclonic Epilepsy 11
OMIM ID 618876
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene SEMA6B
Associated tissues -
Disease features -
Remarks -


Individuals

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00000785 Kohei Hamanaka et al.(2020) F Malaysia - - - - EPM11 - SEMA6B SEMA6B 1 1 Nur Aisyah Athirah
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