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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
movement disease
Summary
- Definition
- A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
- Super Class
- brain disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 5538 | PPT1 | palmitoyl-protein thioesterase 1 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 5660 | PSAP | prosaposin | |
| 5728 | PTEN | phosphatase and tensin homolog | |
| 6448 | SGSH | N-sulfoglucosamine sulfohydrolase | |
| 6515 | SLC2A3 | solute carrier family 2 member 3 | |
| 7915 | ALDH5A1 | aldehyde dehydrogenase 5 family member A1 | |
| 8803 | SUCLA2 | succinate-CoA ligase ADP-forming subunit beta | |
| 22854 | NTNG1 | netrin G1 | |
| 23556 | PIGN | phosphatidylinositol glycan anchor biosynthesis class N |
Related Glycoprotein
