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Mammalian Phenotype (MP): abnormal placental labyrinth vasculature 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:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + + 4:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + 3:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + + 3:   abnormal extraembryonic tissue morphology [MP:0002086] <17>(13|18) (16|4|3)
+ + 2:   abnormal placenta morphology [MP:0001711] <12>(6|9) (9|4|2)
+ + 2:   abnormal blood vessel morphology [MP:0001614] <29>(31|38) (36|27|24)
+ 1:   abnormal placenta labyrinth morphology [MP:0001716] <7>(2|3) (3|0|0)
+ 1:   abnormal placenta vasculature [MP:0003231] <2>(1|2) (1|0|0)
0:   abnormal placental labyrinth vasculature morphology [MP:0008803](0|1) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain0.0002307Direct


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