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Phenotypic Abnormality (PA): Babinski sign

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormality of movement [HP:0100022] <19>(23|25) (25|14|3)
+ + + 3:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + 2:   Upper motor neuron dysfunction [HP:0002493] <4>(9|15) (13|8|4)
+ + 2:   Abnormal reflex [HP:0031826] <5>(6|9) (6|6|1)
+ 1:   Abnormal superficial reflex [HP:0031828] <3>(1|0) (1|0|0)
+ 1:   Abnormal pyramidal sign [HP:0007256] <5>(2|2) (2|1|0)
0:   Babinski sign [HP:0003487](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Cysteine proteinases0.0001188Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Cysteine proteinases0.00005526Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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