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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 |
|---|---|---|---|
| 2581 | GALC | galactosylceramidase | |
| 2592 | GALT | galactose-1-phosphate uridylyltransferase | |
| 2720 | GLB1 | galactosidase beta 1 | |
| 3295 | HSD17B4 | hydroxysteroid 17-beta dehydrogenase 4 | |
| 4099 | MAG | myelin associated glycoprotein | |
| 4968 | OGG1 | 8-oxoguanine DNA glycosylase | |
| 5130 | PCYT1A | phosphate cytidylyltransferase 1A, choline | |
| 5160 | PDHA1 | pyruvate dehydrogenase E1 subunit alpha 1 | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | |
| 5291 | PIK3CB | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta |
Related Glycoprotein
