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Mammalian Phenotype (MP): increased mean corpuscular hemoglobin

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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)
+ + + + + + + + + 9:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + + + 6:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(57|86) (66|47|21)
+ + + + + 5:   abnormal hematopoietic cell morphology [MP:0013656] <9>(48|77) (60|43|18)
+ + + + + 5:   abnormal myeloid cell morphology [MP:0013658] <8>(19|41) (26|23|8)
+ + + + 4:   abnormal erythroid lineage cell morphology [MP:0013659] <5>(8|14) (9|12|6)
+ + + + 4:   abnormal blood cell morphology [MP:0013657] <4>(31|49) (37|35|14)
+ + + 3:   abnormal erythrocyte morphology [MP:0002447] <30>(6|12) (7|10|4)
+ + 2:   abnormal hemoglobin [MP:0001588] <3>(2|7) (4|7|3)
+ 1:   abnormal mean corpuscular hemoglobin [MP:0001589] <2>(2|4) (2|3|2)
0:   increased mean corpuscular hemoglobin [MP:0005561](0|0) (0|0|0)