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bilateral perisylvian polymicrogyria
Summary
- Definition
- A polymicrogyria that is characterized by strikingly restricted polymicrogyria limited to the cortex surrounding the Sylvian fissure and that has_material_basis_in homozygous deletion of one 15-bp tandem repeat in a regulatory region of exon 1m of the ADGRG1 gene on chromosome 16q21.
- Super Class
- polymicrogyria
External Links
- Disease Ontology
- DOID:0080924
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001320 | Cerebellar vermis hypoplasia |
| HP:0000252 | Microcephaly |
| HP:0001328 | Specific learning disability |
| HP:0000767 | Pectus excavatum |
| HP:0001511 | Intrauterine growth retardation |
| HP:0000365 | Hearing impairment |
| HP:0001260 | Dysarthria |
| HP:0002020 | Gastroesophageal reflux |
| HP:0001250 | Seizure |
| HP:0001349 | Facial diplegia |
