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Phenotypic Abnormality (PA): Lymphadenitis

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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 cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + + 3:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + 2:   Abnormal inflammatory response [HP:0012647] <2>(17|20) (18|11|3)
+ + 2:   Abnormality of the lymphatic system [HP:0100763] <7>(9|19) (15|8|5)
+ 1:   Increased inflammatory response [HP:0012649] <27>(15|18) (16|9|3)
+ 1:   Abnormality of the lymph nodes [HP:0002733] <6>(3|9) (7|5|2)
0:   Lymphadenitis [HP:0002840](0|0) (0|0|0)