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Phenotypic Abnormality (PA): Abnormal apolipoprotein level

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + 2:   Abnormal circulating metabolite concentration [HP:0032180] <12>(30|31) (31|14|4)
+ 1:   Abnormal circulating protein level [HP:0010876] <41>(3|9) (4|5|2)
0:   Abnormal apolipoprotein level [HP:0025201] <4>(0|0) (0|0|0)
- 1:   Decreased apolipoprotein AI level [HP:0031799](0|0) (0|0|0)
- 1:   Elevated apolipoprotein A-II level [HP:0031800](0|0) (0|0|0)
- 1:   Elevated apolipoprotein A-IV level [HP:0025202](0|0) (0|0|0)
- 1:   Elevated apolipoprotein B level [HP:0031798](0|0) (0|0|0)