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Phenotypic Abnormality (PA): Hemiparesis

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + 5:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + + 4:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + + 3:   Upper motor neuron dysfunction [HP:0002493] <4>(9|15) (13|8|4)
+ + 2:   Weakness due to upper motor neuron dysfunction [HP:0010549] <3>(1|4) (4|2|2)
+ 1:   Hemiplegia/hemiparesis [HP:0004374] <2>(1|3) (2|2|2)
0:   Hemiparesis [HP:0001269](0|0) (0|0|1)


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Supra-domain (including individual superfamily)

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.0001887Direct