mitochondrial DNA depletion syndrome 19

Summary
Definition
A mitochondrial DNA depletion syndrome that has_material_basis_in compound heterozygous mutation in the SLC25A10 gene on chromosome 17q25.3.
Super Class
autosomal recessive disease mitochondrial DNA depletion syndrome
External Links
Disease Ontology
DOID:0070450
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1468 SLC25A10 solute carrier family 25 member 10
Displaying 1 entry
Gene ID Gene Symbol Description Source
27376 Slc25a10 solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10

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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