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Phenotypic Abnormality (PA): Mitochondrial depletion

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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:   Abnormal cellular phenotype [HP:0025354] <3>(10|10) (13|3|0)
+ + + + 4:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + + 3:   Abnormal cellular physiology [HP:0011017] <16>(10|10) (13|3|0)
+ + 2:   Abnormality of the mitochondrion [HP:0012103] <2>(5|3) (7|1|0)
+ 1:   Abnormality of mitochondrial metabolism [HP:0003287] <14>(5|3) (7|1|0)
0:   Mitochondrial depletion [HP:0030059](0|0) (0|0|0)