1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111325 | juvenile myoclonic epilepsy 10 | A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:331 | central nervous system disease | A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. |