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Mammalian Phenotype (MP): abnormal vitelline vein 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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + + 4:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + + 3:   abnormal cardiovascular development [MP:0002925] <10>(16|35) (25|19|9)
+ + + 3:   abnormal blood vessel morphology [MP:0001614] <29>(31|38) (36|27|24)
+ + + 3:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + 2:   abnormal vascular development [MP:0000259] <9>(13|24) (18|13|5)
+ + 2:   abnormal vein morphology [MP:0002725] <17>(2|2) (2|4|2)
+ + 2:   abnormal angiogenesis [MP:0000260] <8>(9|15) (12|9|4)
+ + 2:   abnormal extraembryonic tissue morphology [MP:0002086] <17>(13|18) (16|4|3)
+ 1:   abnormal vein development [MP:0003411] <3>(2|2) (2|2|0)
+ 1:   abnormal vitelline vasculature morphology [MP:0003229] <4>(1|4) (1|0|0)
0:   abnormal vitelline vein morphology [MP:0010666] <2>(0|0) (0|0|0)
- 1:   abnormal vitelline vein connection [MP:0013859](0|0) (0|0|0)
- 1:   abnormal vitelline vein topology [MP:0013986](0|0) (0|0|0)