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Mammalian Phenotype (MP): abnormal motile cilium 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + 2:   abnormal cell morphology [MP:0000358] <12>(19|19) (22|9|2)
+ 1:   abnormal cilium morphology [MP:0013202] <2>(3|2) (3|3|1)
0:   abnormal motile cilium morphology [MP:0013206] <4>(0|0) (0|0|0)
- 1:   abnormal sperm flagellum morphology [MP:0008892] <15>(0|0) (0|0|0)
- 1:   abnormal ependyma motile cilium morphology [MP:0011059] <2>(0|0) (0|0|0)
- 1:   abnormal oviduct epithelium motile cilium morphology [MP:0011644] <1>(0|0) (0|0|0)
- 1:   abnormal respiratory motile cilium morphology [MP:0011050] <1>(0|0) (0|0|0)