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Phenotypic Abnormality (PA): Tall stature

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Growth abnormality [HP:0001507] <6>(29|47) (34|27|21)
+ 1:   Abnormality of body height [HP:0000002] <3>(9|13) (9|7|8)
0:   Tall stature [HP:0000098] <5>(0|1) (0|1|0)
- 1:   Birth length greater than 97th percentile [HP:0003517](0|0) (0|0|0)
- 1:   Disproportionate tall stature [HP:0001519](0|0) (0|0|0)
- 1:   Overgrowth [HP:0001548](0|0) (0|0|0)
- 1:   Proportionate tall stature [HP:0011407](0|0) (0|0|0)
- 1:   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) domain0.03155Inherited


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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
  • 0.00007868Direct