Details of Disease | DrugMAP

General Information of Disease (ID: DISWZZ5G)

Disease Name	Obsolete combined oxidative phosphorylation defect type 29
Disease Hierarchy	DIS01GPL: Grass pollen hypersensitivity DISWZZ5G: Obsolete combined oxidative phosphorylation defect type 29

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
TXN2	OTE9A5XQ	Supportive	Autosomal recessive	[1]
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References

1	Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration. Brain. 2016 Feb;139(Pt 2):346-54. doi: 10.1093/brain/awv350. Epub 2015 Dec 1.