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Mammalian Phenotype (MP): abnormal liver sinusoid morphology

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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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   liver/biliary system phenotype [MP:0005370] <2>(37|39) (41|19|10)
+ + + + 4:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + 3:   abnormal hepatobiliary system morphology [MP:0002138] <6>(25|32) (28|15|5)
+ + + 3:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + 2:   abnormal liver parenchyma morphology [MP:0008986] <3>(2|2) (2|2|0)
+ + 2:   abnormal liver morphology [MP:0000598] <26>(23|28) (26|13|5)
+ + 2:   abnormal blood vessel morphology [MP:0001614] <29>(31|38) (36|27|24)
+ 1:   abnormal liver vasculature morphology [MP:0009820] <3>(4|4) (4|0|0)
+ 1:   abnormal liver lobule morphology [MP:0008987] <5>(2|2) (2|2|0)
0:   abnormal liver sinusoid morphology [MP:0008989] <2>(0|0) (0|0|0)
- 1:   abnormal Kupffer cell morphology [MP:0008114](0|0) (0|0|0)
- 1:   enlarged liver sinusoidal spaces [MP:0000602](0|0) (0|0|0)