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Mammalian Phenotype (MP): impaired osteoblast differentiation

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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>
+ + + + 4:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   abnormal bone structure [MP:0003795] <17>(17|23) (22|14|6)
+ + + 3:   abnormal skeleton morphology [MP:0005508] <15>(41|59) (47|38|25)
+ + 2:   abnormal osteoblast morphology [MP:0004986] <3>(2|1) (3|0|0)
+ + 2:   abnormal skeleton development [MP:0002113] <13>(6|14) (6|5|2)
+ + 2:   abnormal cell differentiation [MP:0005076] <25>(11|17) (13|5|4)
+ 1:   abnormal osteoblast differentiation [MP:0008395] <2>(0|0) (0|0|0)
0:   impaired osteoblast differentiation [MP:0011711] <1>(0|0) (0|0|0)
- 1:   arrested osteoblast differentiation [MP:0011712](0|0) (0|0|0)