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Mammalian Phenotype (MP): abnormal skeletal muscle 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:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ + 2:   abnormal cell death [MP:0000313] <5>(29|41) (33|15|5)
+ 1:   abnormal muscle physiology [MP:0002106] <23>(25|33) (27|16|11)
+ 1:   abnormal apoptosis [MP:0001648] <30>(27|38) (30|13|5)
0:   abnormal skeletal muscle cell apoptosis [MP:0020239] <2>(0|0) (0|0|0)
- 1:   decreased skeletal muscle cell apoptosis [MP:0020241](0|0) (0|0|0)
- 1:   increased skeletal muscle cell apoptosis [MP:0020240](0|0) (0|0|0)