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basal ganglia disease
Summary
- Definition
- A brain disease that is characterized by dysfunctional movement, located_in basal ganglia that has_material_basis_in diseased components of the basal ganglia and associated neural circuits.
- Super Class
- brain disease
External Links
- Disease Ontology
- DOID:679
- Mondo Disease Ontology
- MeSH
- UMLS
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1737 | DLAT | dihydrolipoamide S-acetyltransferase | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 2572 | GAD2 | glutamate decarboxylase 2 | |
| 2639 | GCDH | glutaryl-CoA dehydrogenase | |
| 2731 | GLDC | glycine decarboxylase | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 3251 | HPRT1 | hypoxanthine phosphoribosyltransferase 1 | |
| 4594 | MMUT | methylmalonyl-CoA mutase | |
| 5160 | PDHA1 | pyruvate dehydrogenase E1 subunit alpha 1 | |
| 5319 | PLA2G1B | phospholipase A2 group IB |
Related Glycoprotein
