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Mammalian Phenotype (MP): absent erythroid progenitor cell

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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>
+ + + + + 5:   abnormal hematopoietic cell morphology [MP:0013656] <9>(48|77) (60|43|18)
+ + + + + 5:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + 4:   abnormal myeloid cell morphology [MP:0013658] <8>(19|41) (26|23|8)
+ + + + 4:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(57|86) (66|47|21)
+ + + 3:   abnormal bone marrow cell morphology/development [MP:0002398] <8>(3|8) (6|6|0)
+ + + 3:   abnormal erythroid lineage cell morphology [MP:0013659] <5>(8|14) (9|12|6)
+ + 2:   abnormal erythroid progenitor cell morphology [MP:0008801] <2>(1|1) (1|1|0)
+ 1:   decreased erythroid progenitor cell number [MP:0008973] <1>(1|1) (1|1|0)
0:   absent erythroid progenitor cell [MP:0000216](0|0) (0|0|0)