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Phenotypic Abnormality (PA): Renal cortical necrosis

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + + + + 5:   Abnormality of the urinary system [HP:0000079] <4>(38|41) (45|15|7)
+ + + + 4:   Abnormality of the upper urinary tract [HP:0010935] <2>(21|22) (22|7|3)
+ + + 3:   Abnormality of the kidney [HP:0000077] <3>(17|16) (18|6|3)
+ + 2:   Abnormal renal morphology [HP:0012210] <26>(14|11) (14|4|1)
+ 1:   Abnormal renal cortex morphology [HP:0011035] <6>(4|5) (4|2|0)
0:   Renal cortical necrosis [HP:0025418](0|0) (0|0|0)