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Mammalian Phenotype (MP): abnormal glial cell apoptosis

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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>
+ + + + 4:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ + 2:   abnormal cell death [MP:0000313] <5>(29|41) (33|15|5)
+ 1:   abnormal glial cell physiology [MP:0003690] <5>(2|2) (3|0|0)
+ 1:   abnormal apoptosis [MP:0001648] <30>(27|38) (30|13|5)
0:   abnormal glial cell apoptosis [MP:0010170] <3>(0|0) (0|0|0)
- 1:   abnormal astrocyte apoptosis [MP:0010204](0|0) (0|0|0)
- 1:   abnormal oligodendrocyte apoptosis [MP:0010205](0|0) (0|0|0)
- 1:   abnormal radial glial cell apoptosis [MP:0020392](0|0) (0|0|0)