complex cortical dysplasia with other brain malformations 10 Disease Ontology Browser

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Disease Ontology Browser

complex cortical dysplasia with other brain malformations 10 (DOID:0061143)
Alliance: disease page
Synonyms: CDCBM10
Alt IDs: OMIM:618677
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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