Epilepsy due to chromosomal disorders (Q86438): Difference between revisions
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| description / pt-br | description / pt-br | ||
Epilepsia devida a duplicações, deleções ou rupturas em ponto de interrupção de cromossomo, em que os fenótipos mais comuns são deficiência intelectual e/ou características dismórficas. | |||
| description / en | description / en | ||
Epilepsy due to chromosome duplications, deletions or breakpoint disruptions whose most common phenotypes are mental retardation and/or dysmorphic features. | |||
Revision as of 11:50, 15 August 2026
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. |
