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Phenotypic Abnormality (PA): Recurrent urinary tract infections

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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)
+ + + + 4:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + + 3:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + 2:   Abnormality of the urinary system [HP:0000079] <4>(38|41) (45|15|7)
+ + 2:   Unusual infection [HP:0032101] <11>(15|19) (17|6|0)
+ 1:   Recurrent infections [HP:0002719] <15>(6|12) (8|4|0)
+ 1:   Abnormality of the urinary system physiology [HP:0011277] <3>(23|26) (28|9|5)
0:   Recurrent urinary tract infections [HP:0000010] <2>(0|1) (0|0|0)
- 1:   Recurrent cystitis [HP:0012786](0|0) (0|0|0)
- 1:   Recurrent pyelonephritis [HP:0012787](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
RecA protein-like (ATPase-domain)0.0003435Direct


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