Search Ontology:
Human Disease
bilateral frontoparietal polymicrogyria
- Term ID
- DOID:0080922
- Synonyms
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- CDCBM14A
- complex cortical dysplasia with other brain malformations 14A
- 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. https://pubmed.ncbi.nlm.nih.gov/34863467/
- References
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- GARD:10784
- MIM:606854
- NCI:C148367
- Ontology
- Human Disease ( DOID:0080922 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models