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Mammalian Phenotype (MP): abnormal bone marrow 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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + 3:   abnormal immune system morphology [MP:0000685] <3>(51|76) (60|35|18)
+ + 2:   abnormal immune system organ morphology [MP:0002722] <8>(21|31) (26|15|9)
+ 1:   abnormal lymph organ development [MP:0002450] <1>(0|0) (0|0|0)
0:   abnormal bone marrow development [MP:0000168] <1>(0|0) (0|0|0)
- 1:   bone marrow failure [MP:0013776] <1>(0|0) (0|0|0)