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Phenotypic Abnormality (PA): Pes valgus

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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 limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + 2:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ 1:   Abnormality of the foot [HP:0001760] <30>(19|21) (19|12|10)
0:   Pes valgus [HP:0008081](1|1) (1|1|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
vWA-like0.000007448Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Integrin A (or I) domain0.0000003836Direct


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)
vWA-like0.000003262Direct

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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
  • 0.0000000413Direct


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