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Disease Ontology (DO): mitochondrial DNA depletion syndrome 13

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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)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ + 2:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
+ 1:   mitochondrial metabolism disease [DOID:700] <41>(0|0) (0|0|0)
0:   mitochondrial DNA depletion syndrome 13 [DOID:0080131](0|0) (0|0|0)