combined oxidative phosphorylation deficiency 25

Summary
Synonym
  • COXPD25
Definition
A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MARS2 gene on chromosome 2q33.1.
Super Class
autosomal recessive disease combined oxidative phosphorylation deficiency
External Links
Disease Ontology
DOID:0111468
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
92935 MARS2 methionyl-tRNA synthetase 2, mitochondrial

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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