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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
cerebellar disease
Summary
- Definition
- A brain disease that is characterized by damage to brain substance located_in cerebellum; has_symptom ataxia, has_symptom dysarthria, and has_symptom cerebellar cognitive affective syndrome.
- Super Class
- brain disease
External Links
- Disease Ontology
- DOID:2786
- Mondo Disease Ontology
- MeSH
- UMLS
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 43 | ACHE | acetylcholinesterase (Yt blood group) | |
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 410 | ARSA | arylsulfatase A | |
| 847 | CAT | catalase | |
| 1203 | CLN5 | CLN5 intracellular trafficking protein | |
| 1738 | DLD | dihydrolipoamide dehydrogenase | |
| 2026 | ENO2 | enolase 2 | |
| 2548 | GAA | alpha glucosidase | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 2572 | GAD2 | glutamate decarboxylase 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q96EG1 | Arylsulfatase G | |
| Q9GZR5 | Very long chain fatty acid elongase 4 | |
| Q9NY47 | Voltage-dependent calcium channel subunit alpha-2/delta-2 | |
| Q9NYP7 | Very long chain fatty acid elongase 5 | |
| Q9UMR5 | Lysosomal thioesterase PPT2 |
