Miller-Dieker syndrome (Q86804): Difference between revisions
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Revision as of 12:21, 15 August 2026
Miller-Dieker Syndrome is a contiguous gene deletion syndrome of chromosome 17p13.3, characterised by classical lissencephaly (lissencephaly type 1) and distinct facial features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_478783491 |
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| English | Miller-Dieker syndrome |
Miller-Dieker Syndrome is a contiguous gene deletion syndrome of chromosome 17p13.3, characterised by classical lissencephaly (lissencephaly type 1) and distinct facial features. |
