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
Displaying entries 21 - 30 of 35 in total
Gene ID Gene Symbol Description Source
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5373 PMM2 phosphomannomutase 2
5621 PRNP prion protein (Kanno blood group)
6785 ELOVL4 ELOVL fatty acid elongase 4
8398 PLA2G6 phospholipase A2 group VI
9254 CACNA2D2 calcium voltage-gated channel auxiliary subunit alpha2delta 2
9374 PPT2 palmitoyl-protein thioesterase 2
9420 CYP7B1 cytochrome P450 family 7 subfamily B member 1
10908 PNPLA6 patatin like phospholipase domain containing 6

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024