Search Ontology:
Human Disease

bilateral frontoparietal polymicrogyria

Term ID
DOID:0080922
Synonyms
  • 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
Ontology
Human Disease   ( DOID:0080922 )
Relationships
is a type of
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Genes Involved
Zebrafish Models