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Mammalian Phenotype (MP): abnormal notochord 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + 2:   abnormal embryo morphology [MP:0014134] <4>(23|31) (26|14|12)
+ 1:   abnormal embryonic tissue morphology [MP:0002085] <35>(17|21) (19|10|9)
0:   abnormal notochord morphology [MP:0002825] <6>(0|0) (1|0|0)
- 1:   absent notochord [MP:0000932](0|0) (0|0|0)
- 1:   notochord degeneration [MP:0004712](0|0) (0|0|0)
- 1:   persistence of notochord tissue [MP:0004711](0|0) (0|0|0)
- 1:   small notochord [MP:0004710](0|0) (0|0|0)
- 1:   split notochord [MP:0004713](0|0) (0|0|0)
- 1:   truncated notochord [MP:0004714](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
FnI-like domain0.0006764Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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