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Mammalian Phenotype (MP): hepatic peliosis

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children) MP term [MP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   liver/biliary system phenotype [MP:0005370] <2>(37|39) (41|19|10)
+ + + 3:   abnormal hepatobiliary system morphology [MP:0002138] <6>(25|32) (28|15|5)
+ + + 3:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + 2:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + 2:   abnormal liver morphology [MP:0000598] <26>(23|28) (26|13|5)
+ 1:   abnormal liver parenchyma morphology [MP:0008986] <3>(2|2) (2|2|0)
+ 1:   peliosis [MP:0013332] <2>(0|0) (0|0|0)
0:   hepatic peliosis [MP:0013335](0|0) (0|0|0)