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Phenotypic Abnormality (PA): Muscle abnormality related to mitochondrial dysfunction

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ 1:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
0:   Muscle abnormality related to mitochondrial dysfunction [HP:0003800] <4>(0|0) (0|0|0)
- 1:   Depletion of mitochondrial DNA in muscle tissue [HP:0009141] <1>(0|0) (0|0|0)
- 1:   Mitochondrial myopathy [HP:0003737] <1>(0|0) (0|0|0)
- 1:   Cytochrome C oxidase-negative muscle fibers [HP:0003688](0|0) (0|0|0)
- 1:   Subsarcolemmal accumulations of abnormally shaped mitochondria [HP:0003548](0|0) (0|0|0)