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Mammalian Phenotype (MP): abnormal heart position or orientation

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + 2:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ 1:   abnormal heart morphology [MP:0000266] <22>(27|44) (28|25|19)
0:   abnormal heart position or orientation [MP:0006065] <7>(0|1) (0|0|0)
- 1:   atrial situs inversus [MP:0010431](0|0) (0|0|0)
- 1:   dextrocardia [MP:0000644](0|0) (0|0|0)
- 1:   ectopia cordis [MP:0011660](0|0) (0|0|0)
- 1:   left atrial isomerism [MP:0008461](0|0) (0|0|0)
- 1:   mesocardia [MP:0000650](0|0) (0|0|0)
- 1:   right atrial isomerism [MP:0006061](0|0) (0|0|0)
- 1:   superior-inferior ventricles [MP:0011254](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Transforming growth factor (TGF)-beta0.0003348Direct


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