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Disease Ontology (DO): mitochondrial metabolism disease

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ 1:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
0:   mitochondrial metabolism disease [DOID:700] <41>(0|0) (0|0|0)
- 1:   Leigh disease [DOID:3652](0|0) (0|0|0)
- 1:   Pearson syndrome [DOID:0060067](0|0) (0|0|0)
- 1:   Sengers syndrome [DOID:0080132](0|0) (0|0|0)
- 1:   coenzyme Q10 deficiency disease [DOID:0050730](0|0) (0|0|0)
- 1:   combined oxidative phosphorylation deficiency [DOID:0060286](0|0) (0|0|0)
- 1:   cytochrome-c oxidase deficiency disease [DOID:3762](0|0) (0|0|0)
- 1:   deafness dystonia syndrome [DOID:0050757](0|0) (0|0|0)
- 1:   ethylmalonic encephalopathy [DOID:0060640](0|0) (0|0|0)
- 1:   fatal infantile encephalocardiomyopathy [DOID:0050713](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 1 [DOID:0080119](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 11 [DOID:0080129](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 12 [DOID:0080130](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 13 [DOID:0080131](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 2 [DOID:0080120](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 3 [DOID:0080121](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 4a [DOID:0080122](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 4b [DOID:0080123](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 5 [DOID:0080124](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 6 [DOID:0080125](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 7 [DOID:0080126](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 8a [DOID:0080127](0|0) (0|0|0)
- 1:   mitochondrial DNA depletion syndrome 9 [DOID:0080128](0|0) (0|0|0)
- 1:   mitochondrial complex I deficiency [DOID:0060536](0|0) (0|0|0)
- 1:   mitochondrial complex II deficiency [DOID:0060537](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 1 [DOID:0080111](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 2 [DOID:0060351](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 3 [DOID:0080112](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 4 [DOID:0080113](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 5 [DOID:0080114](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 6 [DOID:0080115](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 7 [DOID:0080116](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 8 [DOID:0080117](0|0) (0|0|0)
- 1:   mitochondrial complex III deficiency nuclear type 9 [DOID:0080118](0|0) (0|0|0)
- 1:   mitochondrial complex V (ATP synthase) deficiency nuclear type 2 [DOID:0060331](0|0) (0|0|0)
- 1:   mitochondrial complex V (ATP synthase) deficiency nuclear type 3 [DOID:0060332](0|0) (0|0|0)
- 1:   mitochondrial complex V (ATP synthase) deficiency nuclear type 4 [DOID:0060333](0|0) (0|0|0)
- 1:   mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 [DOID:0050768](0|0) (0|0|0)
- 1:   multiple mitochondrial dysfunctions syndrome 1 [DOID:0080133](0|0) (0|0|0)
- 1:   multiple mitochondrial dysfunctions syndrome 2 [DOID:0080134](0|0) (0|0|0)
- 1:   multiple mitochondrial dysfunctions syndrome 3 [DOID:0080135](0|0) (0|0|0)
- 1:   multiple mitochondrial dysfunctions syndrome 4 [DOID:0080136](0|0) (0|0|0)