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Mammalian Phenotype (MP): abnormal 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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + 2:   mammalian phenotype [MP:0000001] <29>
+ 1:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
0:   abnormal melanocyte morphology [MP:0002877] <9>(0|0) (0|0|0)
- 1:   abnormal melanosome morphology [MP:0005075] <6>(0|0) (0|0|0)
- 1:   abnormal hair follicle melanocyte morphology [MP:0004381] <3>(0|0) (0|0|0)
- 1:   abnormal melanocyte number [MP:0012021] <2>(0|0) (0|0|0)
- 1:   abnormal choroid melanocyte morphology [MP:0010191] <1>(0|0) (0|0|0)
- 1:   abnormal retinal melanocyte morphology [MP:0010190] <1>(0|0) (0|0|0)
- 1:   abnormal strial intermediate cell morphology [MP:0004367] <1>(0|0) (0|0|0)
- 1:   abnormal dermal melanocyte morphology [MP:0009386](0|0) (0|0|0)
- 1:   abnormal epidermal melanocyte morphology [MP:0009388](0|0) (0|0|0)
- 1:   ectopic melanocytes [MP:0010037](0|0) (0|0|0)