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Phenotypic Abnormality (PA): Herpes encephalitis

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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 the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + 3:   Unusual infection [HP:0032101] <11>(15|19) (17|6|0)
+ + 2:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + 2:   Unusual infection by anatomical site [HP:0032158] <2>(9|8) (10|2|0)
+ 1:   Unusual CNS infection [HP:0011450] <5>(9|7) (10|2|0)
0:   Herpes encephalitis [HP:0020098](0|0) (0|0|0)