OBO ID: DOID:0060469 |
Term Name: | Miller-Dieker lissencephaly syndrome | Search Ontology: | |
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Definition: | A syndrome characterized by classical lissencephaly and distinct facial features and has_material_basis_in submicroscopic deletions of 17p13.3, including the LIS1 gene. (4) | ||
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Ontology: | Human Disease ( DOID:0060469 ) |
OTHER Miller-Dieker lissencephaly syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
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