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Mammalian Phenotype (MP): increased hepatoblastoma incidence

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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)
+ + + + + + + + 8:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   neoplasm [MP:0002006] <2>(32|37) (38|18|7)
+ + + + + + 6:   altered tumor susceptibility [MP:0002166] <3>(25|29) (30|11|3)
+ + + + + 5:   abnormal tumor incidence [MP:0002019] <6>(25|29) (30|11|3)
+ + + + 4:   increased tumor incidence [MP:0002020] <3>(25|27) (30|10|3)
+ + + + 4:   abnormal classified tumor incidence [MP:0020188] <3>(20|19) (26|7|1)
+ + + + 4:   liver/biliary system phenotype [MP:0005370] <2>(37|39) (41|19|10)
+ + + + 4:   abnormal organ/body region tumor incidence [MP:0013152] <2>(21|24) (24|8|3)
+ + + 3:   increased organ/body region tumor incidence [MP:0010274] <14>(21|24) (24|8|3)
+ + + 3:   increased classified tumor incidence [MP:0010273] <19>(20|19) (26|7|1)
+ + + 3:   abnormal hepatobiliary system morphology [MP:0002138] <6>(25|32) (28|15|5)
+ + 2:   increased hepatobiliary system tumor incidence [MP:0010297] <2>(1|3) (1|1|0)
+ + 2:   increased malignant tumor incidence [MP:0002018] <5>(7|11) (10|6|0)
+ 1:   increased blastoma incidence [MP:0008021] <6>(1|1) (1|0|0)
+ 1:   increased liver tumor incidence [MP:0008019] <6>(1|3) (1|1|0)
0:   increased hepatoblastoma incidence [MP:0010054](0|0) (0|0|0)