Mitochondrial complex v (atp synthase) deficiency, nuclear type 2

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Subtype of: Mitochondrial complex deficiency · Mitochondrial complex v (atp synthase) deficiency, nuclear type
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2
MONDO_0013546
TMEM70 Causal
24485043 21147908 20335238 18953340 27604308 26550569 24740313
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Mitochondrial complex v (atp synthase) deficiency, nuclear type 2.
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Mitochondrial encephalocardiomyopathy 1 shared geneTMEM70 Related via 1 shared gene including TMEM70. Oligohydramnios 1 shared geneTMEM70 Related via 1 shared gene including TMEM70. Mitochondrial complex v (atp synthase) deficiency, nuclear type 1 shared geneTMEM70 Related via 1 shared gene including TMEM70. Intrauterine growth restriction 1 shared geneTMEM70 Related via 1 shared gene including TMEM70. Anhydramnios 1 shared geneTMEM70 Related via 1 shared gene including TMEM70.