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Standards Ontologies Notations
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 31 - 35 of 35 in total
Gene ID Gene Symbol Description Source
22901 ARSG arylsulfatase G
55331 ACER3 alkaline ceramidase 3
57704 GBA2 glucosylceramidase beta 2
60481 ELOVL5 ELOVL fatty acid elongase 5
79644 SRD5A3 steroid 5 alpha-reductase 3
Related Glycoprotein
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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