Epilepsy due to chromosomal disorders (Q86438): Difference between revisions
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13 August 2026
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Latest 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 |
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| 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. |
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CID11:ID_1347107851
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dki-india-ID_1347107851
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Concluído
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13 August 2026
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