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Phenotypic Abnormality (PA): Depletion of mitochondrial DNA in liver

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|14|4)
+ + 2:   Abnormality of the liver [HP:0001392] <4>(17|12) (17|7|0)
+ 1:   Abnormal liver morphology [HP:0410042] <25>(13|9) (13|4|0)
0:   Depletion of mitochondrial DNA in liver [HP:0006581](0|0) (0|0|0)