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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01369 | ATP synthase deficiency | ATP synthase deficiency is mitochondrial disease caused by inborn defects in the mitochondrial F1Fo-ATP synthase (respiratory chain complex V). Many patients die within a few months or years. It has been ... | Inherited metabolic disorder, Mitochondrial disease |
(MC5DN1) ATPAF2 [HSA:91647] [KO:K07556] (MC5DN2) TMEM70 [HSA:54968] [KO:K17966] (MC5DN3) ATP5F1E [HSA:514] [KO:K02135] (MC5DN4A/4B) ATP5F1A [HSA:498] [KO:K02132] (MC5DN5) ATP5F1D [HSA:513] [KO:K02134] (MC5DN6) ATP5MK [HSA:84833] [KO:K18194] (MC5DN7) ATP5PO [HSA:539] [KO:K02137] (MC5DM1/NARP/MIBSN) ATP6 [HSA:4508] [KO:K02126] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |