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Mammalian Phenotype (MP): abnormal epidermal melanocyte morphology

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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)
+ + + + + 5:   integument phenotype [MP:0010771] <5>(46|64) (53|34|18)
+ + + + 4:   abnormal skin morphology [MP:0002060] <16>(19|26) (24|13|8)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   abnormal skin coloration [MP:0011239] <1>(0|0) (1|1|0)
+ + 2:   abnormal skin pigmentation [MP:0002095] <11>(0|0) (1|1|0)
+ + 2:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
+ 1:   abnormal epidermal pigmentation [MP:0009387] <1>(0|0) (0|0|0)
+ 1:   abnormal melanocyte morphology [MP:0002877] <9>(0|0) (0|0|0)
0:   abnormal epidermal melanocyte morphology [MP:0009388](0|0) (0|0|0)