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Mammalian Phenotype (MP): absent common myeloid progenitor cells

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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>
+ + + + + 5:   abnormal blood cell morphology/development [MP:0002429] <3>(26|35) (28|24|9)
+ + + + + 5:   abnormal blood cell morphology [MP:0013657] <4>(31|49) (37|35|14)
+ + + + + 5:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + 4:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + + 4:   abnormal hemopoiesis [MP:0013693] <2>(25|34) (27|24|9)
+ + + 3:   abnormal bone marrow cell number [MP:0000172] <3>(0|0) (0|0|0)
+ + + 3:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|77) (60|43|18)
+ + + 3:   abnormal bone marrow cell morphology/development [MP:0002398] <8>(3|8) (6|6|0)
+ + + 3:   abnormal definitive hematopoiesis [MP:0002123] <4>(24|34) (26|24|9)
+ + 2:   abnormal common myeloid progenitor cell morphology [MP:0006410] <2>(1|1) (1|2|0)
+ + 2:   decreased bone marrow cell number [MP:0000333] <1>(0|0) (0|0|0)
+ 1:   absent bone marrow cell [MP:0000175] <1>(0|0) (0|0|0)
+ 1:   decreased common myeloid progenitor cell number [MP:0008813] <1>(0|0) (0|0|0)
0:   absent common myeloid progenitor cells [MP:0000239](0|0) (0|0|0)