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Mammalian Phenotype (MP): small interparietal bone

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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)
+ + + + + + + + 8:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + + + + + 6:   abnormal skeleton morphology [MP:0005508] <15>(41|59) (47|38|25)
+ + + + + + 6:   craniofacial phenotype [MP:0005382] <1>(20|36) (24|17|10)
+ + + + + 5:   abnormal axial skeleton morphology [MP:0002114] <4>(24|40) (25|21|14)
+ + + + + 5:   abnormal craniofacial morphology [MP:0000428] <5>(20|36) (24|17|10)
+ + + + 4:   abnormal craniofacial bone morphology [MP:0002116] <3>(16|25) (16|13|7)
+ + + 3:   abnormal cranium morphology [MP:0000438] <11>(16|25) (16|13|7)
+ + 2:   abnormal neurocranium morphology [MP:0000074] <11>(5|5) (5|3|0)
+ 1:   abnormal interparietal bone morphology [MP:0000077] <3>(0|1) (0|0|0)
0:   small interparietal bone [MP:0004384] <1>(0|1) (0|0|0)
- 1:   interparietal bone hypoplasia [MP:0004385](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Transforming growth factor (TGF)-beta0.000003095Direct


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