basal ganglia disease

Summary
Definition
A brain disease that is characterized by dysfunctional movement, located_in basal ganglia that has_material_basis_in diseased components of the basal ganglia and associated neural circuits.
Super Class
brain disease
External Links
Disease Ontology
DOID:679
Mondo Disease Ontology
MeSH
UMLS
Related Genes
Displaying entries 1 - 10 of 17 in total
Gene ID Gene Symbol Description Source
1737 DLAT dihydrolipoamide S-acetyltransferase
2571 GAD1 glutamate decarboxylase 1
2572 GAD2 glutamate decarboxylase 2
2639 GCDH glutaryl-CoA dehydrogenase
2731 GLDC glycine decarboxylase
2752 GLUL glutamate-ammonia ligase
3251 HPRT1 hypoxanthine phosphoribosyltransferase 1
4594 MMUT methylmalonyl-CoA mutase
5160 PDHA1 pyruvate dehydrogenase E1 subunit alpha 1
5319 PLA2G1B phospholipase A2 group IB

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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