Miller-Dieker syndrome (Q86804): Difference between revisions

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Latest 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
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.