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General Information
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| Term |
bilateral perisylvian polymicrogyria |
ID (Ontology) |
DOID:0080924 (Human Disease) |
| Definition |
A polymicrogyria that is characterized by strikingly restricted polymicrogyria limited to the cortex surrounding the Sylvian fissure and that has_material_basis_in homozygous deletion of one 15-bp tandem repeat in a regulatory region of exon 1m of the ADGRG1 gene on chromosome 16q21. |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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bilateral perisylvian polymicrogyria | 2 | for disease ribbon | bilateral perisylvian polymicrogyria | 2 | model of | bilateral perisylvian polymicrogyria | 2 |
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