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Phenotypic Abnormality (PA): EMG: neuropathic changes

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ 1:   EMG abnormality [HP:0003457] <10>(4|3) (4|2|0)
0:   EMG: neuropathic changes [HP:0003445] <1>(0|0) (0|0|0)
- 1:   EMG: chronic denervation signs [HP:0003444](0|0) (0|0|0)