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Phenotypic Abnormality (PA): Nasal polyposis

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormality of the nose [HP:0000366] <19>(12|16) (15|7|3)
+ 1:   Abnormality of the nasal mucosa [HP:0000433] <2>(0|1) (0|0|1)
0:   Nasal polyposis [HP:0100582](0|1) (0|0|1)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tetratricopeptide repeat (TPR)0.0004082Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52540,52540,52540
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 0.000005859Direct