Epilepsy due to chromosomal disorders (Q86438)
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Epilepsy due to chromosome duplications, deletions or breakpoint disruptions whose most common phenotypes are mental retardation and/or dysmorphic features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1347107851 |
||
| English | Epilepsy due to chromosomal disorders |
Epilepsy due to chromosome duplications, deletions or breakpoint disruptions whose most common phenotypes are mental retardation and/or dysmorphic features. |
