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Phenotypic Abnormality (PA): Halitosis

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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:   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 mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ 1:   Constitutional symptom [HP:0025142] <12>(8|16) (11|7|3)
+ 1:   Abnormal oral physiology [HP:0031815] <7>(2|3) (2|1|1)
0:   Halitosis [HP:0100812] <1>(0|1) (0|0|1)
- 1:   Fetor hepaticus [HP:0032142](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tetratricopeptide repeat (TPR)0.0001761Direct


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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
  • 0.000003379Direct