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Mammalian Phenotype (MP): abnormal ependyma 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:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ 1:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
0:   abnormal ependyma morphology [MP:0002653] <3>(0|0) (0|0|0)
- 1:   abnormal ependyma motile cilium morphology [MP:0011059] <2>(0|0) (0|0|0)
- 1:   abnormal brain ependyma morphology [MP:0010152] <1>(0|0) (0|0|0)
- 1:   abnormal spinal cord ependymal layer morphology [MP:0010151] <1>(0|0) (0|0|0)