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Phenotypic Abnormality (PA): Sinusitis

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + 3:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + + 3:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + 2:   Abnormal inflammatory response [HP:0012647] <2>(17|20) (18|11|3)
+ + 2:   Abnormality of facial skeleton [HP:0011821] <14>(4|4) (5|6|9)
+ 1:   Abnormality of the paranasal sinuses [HP:0000245] <8>(0|1) (0|0|1)
+ 1:   Increased inflammatory response [HP:0012649] <27>(15|18) (16|9|3)
0:   Sinusitis [HP:0000246] <3>(0|0) (0|0|1)
- 1:   Acute sinusitis [HP:0000255](0|0) (0|0|0)
- 1:   Chronic sinusitis [HP:0011109](0|0) (0|0|1)
- 1:   Recurrent sinusitis [HP:0011108](0|0) (0|0|0)


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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
  • 0.0002059Direct