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Mammalian Phenotype (MP): increased cutaneous melanoma 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> #Domains
(Superfamily|Family)
#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:   abnormal classified tumor incidence [MP:0020188] <3>(20|19) (26|7|1)
+ + + + 4:   abnormal organ/body region tumor incidence [MP:0013152] <2>(21|24) (24|8|3)
+ + + + 4:   increased tumor incidence [MP:0002020] <3>(25|27) (30|10|3)
+ + + 3:   increased classified tumor incidence [MP:0010273] <19>(20|19) (26|7|1)
+ + + 3:   increased organ/body region tumor incidence [MP:0010274] <14>(21|24) (24|8|3)
+ + + 3:   integument phenotype [MP:0010771] <5>(46|64) (53|34|18)
+ + 2:   abnormal skin morphology [MP:0002060] <16>(19|26) (24|13|8)
+ + 2:   increased integument system tumor incidence [MP:0010293] <3>(4|7) (7|5|2)
+ + 2:   increased malignant tumor incidence [MP:0002018] <5>(7|11) (10|6|0)
+ 1:   increased melanoma incidence [MP:0010275] <2>(0|0) (0|0|0)
+ 1:   increased skin tumor incidence [MP:0010300] <9>(3|3) (6|1|0)
0:   increased cutaneous melanoma incidence [MP:0010322](0|0) (0|0|0)