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Phenotypic Abnormality (PA): Chronic bronchitis

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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 the respiratory system [HP:0002086] <3>(30|35) (38|24|21)
+ + + + 4:   Abnormal respiratory system morphology [HP:0012252] <5>(20|25) (26|18|17)
+ + + 3:   Abnormal lung morphology [HP:0002088] <28>(11|18) (18|11|7)
+ + 2:   Respiratory tract infection [HP:0011947] <3>(2|7) (3|3|1)
+ 1:   Bronchitis [HP:0012387] <3>(0|2) (1|1|1)
0:   Chronic bronchitis [HP:0004469](0|1) (0|0|1)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tetratricopeptide repeat (TPR)0.0002532Direct


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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
  • 0.000003903Direct