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Phenotypic Abnormality (PA): Toe walking

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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 nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + 2:   Abnormality of movement [HP:0100022] <19>(23|25) (25|14|3)
+ 1:   Gait disturbance [HP:0001288] <22>(5|4) (8|2|1)
0:   Toe walking [HP:0040083](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)
46966,46966,46966
  • 46966 - Spectrin repeat
  • 46966 - Spectrin repeat
  • 46966 - Spectrin repeat
  • 0.0005619Direct