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Phenotypic Abnormality (PA): Distal joint laxity

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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 skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal physiology [HP:0011843] <8>(17|23) (17|15|15)
+ + 2:   Abnormality of joint mobility [HP:0011729] <6>(16|21) (16|15|15)
+ 1:   Joint laxity [HP:0001388] <2>(1|2) (1|1|0)
0:   Distal joint laxity [HP:0020152](1|1) (1|1|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
vWA-like0.0001684Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Integrin A (or I) domain0.00003203Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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-like0.00007953Direct

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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
  • 0.000000000374Direct


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