Mitochondrial complex v (atp synthase) deficiency, nuclear type 1

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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 1
MONDO_0011421
ATPAF2 Causal
27604308 19933271 14757859
Open Targets —
All1 Causal1 Unknown0
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Mitochondrial complex v (atp synthase) deficiency, nuclear type 1 shared geneATPAF2 Related via 1 shared gene including ATPAF2. Mitochondrial complex deficiency 1 shared geneATPAF2 Related via 1 shared gene including ATPAF2. Mitochondrial disease 1 shared geneATPAF2 Related via 1 shared gene including ATPAF2. Schizophrenia 1 shared geneATPAF2 Related via 1 shared gene including ATPAF2.