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Mammalian Phenotype (MP): abnormal melanosome 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)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
+ 1:   abnormal melanocyte morphology [MP:0002877] <9>(0|0) (0|0|0)
0:   abnormal melanosome morphology [MP:0005075] <6>(0|0) (0|0|0)
- 1:   abnormal hair follicle melanin granule morphology [MP:0005072] <5>(0|0) (0|0|0)
- 1:   abnormal hair shaft melanin granule morphology [MP:0008731] <3>(0|0) (0|0|0)
- 1:   abnormal eumelanosome morphology [MP:0013314] <1>(0|0) (0|0|0)
- 1:   abnormal pheomelanosome morphology [MP:0013315] <1>(0|0) (0|0|0)
- 1:   abnormal choroid melanin granule morphology [MP:0010193](0|0) (0|0|0)
- 1:   abnormal retinal melanin granule morphology [MP:0010192](0|0) (0|0|0)