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Phenotypic Abnormality (PA): Asymptomatic hyperammonemia

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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 metabolism/homeostasis [HP:0001939] <16>(75|82) (79|39|16)
+ + + + 4:   Abnormal circulating metabolite concentration [HP:0032180] <12>(30|31) (31|14|4)
+ + + 3:   Abnormal circulating nitrogen compound concentration [HP:0004364] <10>(7|7) (7|3|1)
+ + 2:   Azotemia [HP:0002157] <5>(7|7) (7|3|1)
+ 1:   Hyperammonemia [HP:0001987] <2>(6|5) (6|2|0)
0:   Asymptomatic hyperammonemia [HP:0008162](0|0) (0|0|0)