mitochondrial metabolism disease

Summary
Definition
An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
Super Class
inherited metabolic disorder
External Links
Disease Ontology
DOID:700
Mondo Disease Ontology
MeSH
UMLS
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 32 in total
Gene ID Gene Symbol Description Source
2548 GAA alpha glucosidase
2632 GBE1 1,4-alpha-glucan branching enzyme 1
2678 GGT1 gamma-glutamyltransferase 1
2876 GPX1 glutathione peroxidase 1
3032 HADHB hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
3155 HMGCL 3-hydroxy-3-methylglutaryl-CoA lyase
4594 MMUT methylmalonyl-CoA mutase
4968 OGG1 8-oxoguanine DNA glycosylase
5160 PDHA1 pyruvate dehydrogenase E1 subunit alpha 1
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A

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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