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General Information
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| Term |
complex cortical dysplasia with other brain malformations 10 |
ID (Ontology) |
DOID:0061143 (Human Disease) |
| Definition |
A complex cortical dysplasia with other brain malformations characterized by severely impaired global development associated with abnormalities on brain imaging, including lissencephaly, cortical dysplasia, subcortical heterotopia, and paucity of white matter that has_material_basis_in homozygous or compound heterozygous mutation in the APC2 gene on chromosome 19p13. |
| Also Known As |
"CDCBM10" |
| Comment |
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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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complex cortical dysplasia with other brain malformations 10 | 2 | for disease ribbon | complex cortical dysplasia with other brain malformations 10 | 2 | model of | complex cortical dysplasia with other brain malformations 10 | 2 |
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