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Mammalian Phenotype (MP): abnormal myelopoiesis

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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>
+ + + + + + 6:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + + 5:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + + + 5:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|77) (60|43|18)
+ + + + 4:   abnormal blood cell morphology/development [MP:0002429] <3>(26|35) (28|24|9)
+ + + + 4:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + 4:   abnormal blood cell morphology [MP:0013657] <4>(31|49) (37|35|14)
+ + + 3:   abnormal hemopoiesis [MP:0013693] <2>(25|34) (27|24|9)
+ + + 3:   abnormal immune system morphology [MP:0000685] <3>(51|76) (60|35|18)
+ + 2:   abnormal definitive hematopoiesis [MP:0002123] <4>(24|34) (26|24|9)
+ + 2:   abnormal immune system cell morphology [MP:0000716] <5>(38|63) (48|29|16)
+ 1:   abnormal leukopoiesis [MP:0005460] <3>(19|28) (21|18|8)
0:   abnormal myelopoiesis [MP:0001601] <8>(0|0) (0|0|0)
- 1:   abnormal granulocyte differentiation [MP:0008111] <3>(0|0) (0|0|0)
- 1:   abnormal mast cell differentiation [MP:0005462](0|0) (0|0|0)
- 1:   abnormal monocyte differentiation [MP:0008112](0|0) (0|0|0)
- 1:   abnormal thrombopoiesis [MP:0000228](0|0) (0|0|0)
- 1:   failure of myelopoiesis [MP:0001603](0|0) (0|0|0)
- 1:   impaired myelopoiesis [MP:0001602](0|0) (0|0|0)
- 1:   myeloid hyperplasia [MP:0010373](0|0) (0|0|0)
- 1:   myeloid metaplasia [MP:0013805](0|0) (0|0|0)