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Mammalian Phenotype (MP): abnormal embryonic hematopoiesis

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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:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + 3:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + 3:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|77) (60|43|18)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + 2:   abnormal blood cell morphology [MP:0013657] <4>(31|49) (37|35|14)
+ + 2:   abnormal blood cell morphology/development [MP:0002429] <3>(26|35) (28|24|9)
+ 1:   abnormal hemopoiesis [MP:0013693] <2>(25|34) (27|24|9)
+ 1:   abnormal extraembryonic tissue physiology [MP:0004264] <10>(1|3) (2|2|1)
0:   abnormal embryonic hematopoiesis [MP:0003396] <1>(0|0) (0|0|0)
- 1:   abnormal embryonic erythropoiesis [MP:0004229](0|0) (0|0|0)