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Phenotypic Abnormality (PA): Frequent falls

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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:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + + 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)
+ + 2:   Abnormality of coordination [HP:0011443] <5>(2|3) (7|5|2)
+ 1:   Functional motor deficit [HP:0004302] <7>(1|5) (5|2|0)
+ 1:   Incoordination [HP:0002311] <3>(0|1) (0|1|0)
0:   Frequent falls [HP:0002359](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Integrin A (or I) domain0.0002748Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.00001282Direct