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Mammalian Phenotype (MP): abnormal axial mesoderm

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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:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + + 4:   abnormal embryo morphology [MP:0014134] <4>(23|31) (26|14|12)
+ + + 3:   abnormal embryonic tissue morphology [MP:0002085] <35>(17|21) (19|10|9)
+ + 2:   abnormal germ layer morphology [MP:0014138] <3>(1|3) (1|0|0)
+ 1:   abnormal mesoderm morphology [MP:0014141] <6>(1|2) (1|0|0)
0:   abnormal axial mesoderm [MP:0001684] <4>(0|0) (0|0|0)
- 1:   abnormal prechordal mesoderm morphology [MP:0012275] <1>(0|0) (0|0|0)
- 1:   decreased axial mesoderm size [MP:0012272] <1>(0|0) (0|0|0)
- 1:   abnormal chordamesoderm morphology [MP:0012271](0|0) (0|0|0)
- 1:   increased axial mesoderm size [MP:0012274](0|0) (0|0|0)