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Mammalian Phenotype (MP): abnormal blood vessel lumen formation

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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:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + 3:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + 2:   abnormal cardiovascular development [MP:0002925] <10>(16|35) (25|19|9)
+ + 2:   abnormal blood vessel morphology [MP:0001614] <29>(31|38) (36|27|24)
+ 1:   abnormal vascular development [MP:0000259] <9>(13|24) (18|13|5)
0:   abnormal blood vessel lumen formation [MP:0020373](0|0) (0|0|0)