Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
bilateral frontoparietal polymicrogyria
Summary
- Definition
- A polymicrogyria that is characterized by excessive cortical folding and abnormal cortical layering, that involves the frontoparietal region of the brain and that presents with hypotonia, developmental delay, moderate to severe intellectual disability, pyramidal signs, epileptic seizures, non progressive cerebellar ataxia, dysconjugate gaze and/or strabismus and that has_material_basis_in homozygous mutation in the ADGRG1 gene on chromosome 16q21.
- Super Class
- autosomal recessive disease polymicrogyria
External Links
- Disease Ontology
- DOID:0080922
- Mondo Disease Ontology
- NCI Thesaurus
- OMIM
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001317 | Abnormal cerebellum morphology |
| HP:0007033 | Cerebellar dysplasia |
| HP:0001249 | Intellectual disability |
| HP:0010864 | Intellectual disability, severe |
| HP:0002141 | Gait imbalance |
| HP:0000486 | Strabismus |
| HP:0007266 | Cerebral dysmyelination |
| HP:0002119 | Ventriculomegaly |
| HP:0012110 | Hypoplasia of the pons |
| HP:0001263 | Global developmental delay |
