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Mammalian Phenotype (MP): abnormal vertebral body development

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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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + + + 4:   abnormal axial skeleton morphology [MP:0002114] <4>(24|40) (25|21|14)
+ + + 3:   abnormal vertebral column morphology [MP:0004703] <9>(14|16) (15|11|5)
+ + + 3:   abnormal skeleton morphology [MP:0005508] <15>(41|59) (47|38|25)
+ + 2:   abnormal vertebrae morphology [MP:0000137] <15>(10|10) (11|5|1)
+ + 2:   abnormal skeleton development [MP:0002113] <13>(6|14) (6|5|2)
+ 1:   abnormal vertebrae development [MP:0005225] <4>(0|0) (0|1|0)
+ 1:   abnormal vertebral body morphology [MP:0000141] <7>(1|1) (1|0|0)
0:   abnormal vertebral body development [MP:0005227](0|0) (0|0|0)