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Mammalian Phenotype (MP): abnormal bone marrow cell number

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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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + 2:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ 1:   abnormal bone marrow cell morphology/development [MP:0002398] <8>(3|8) (6|6|0)
0:   abnormal bone marrow cell number [MP:0000172] <3>(0|0) (0|0|0)
- 1:   abnormal myeloid cell number in bone marrow [MP:0013413] <2>(0|0) (0|0|0)
- 1:   decreased bone marrow cell number [MP:0000333] <1>(0|0) (0|0|0)
- 1:   increased bone marrow cell number [MP:0000321](0|0) (0|0|0)