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Disease Ontology Browser
bilateral frontoparietal polymicrogyria (DOID:0080922)
Alliance: disease page
Synonyms: CDCBM14A; complex cortical dysplasia with other brain malformations 14A
Alt IDs: OMIM:606854, NCI:C148367
Definition: A polymicrogyria that is characterized by a global developmental delay with impaired intellectual development, motor delay, poor speech development, and early-onset seizures, often focal or atypical absence and that has_material_basis_in homozygous mutation in the ADGRG1 gene on chromosome 16q21.

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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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03/18/2025
MGI 6.24 		The Jackson Laboratory