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Phenotypic Abnormality (PA): Slender build

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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:   Growth abnormality [HP:0001507] <6>(29|47) (34|27|21)
+ + 2:   Abnormality of body weight [HP:0004323] <4>(9|22) (13|12|3)
+ + 2:   Abnormality of body height [HP:0000002] <3>(9|13) (9|7|8)
+ 1:   Decreased body weight [HP:0004325] <6>(8|15) (9|8|2)
+ 1:   Tall stature [HP:0000098] <5>(0|1) (0|1|0)
0:   Slender build [HP:0001533](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) domain0.0004791Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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
  • 0.0000004Direct