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Mammalian Phenotype (MP): abnormal neural crest 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)
+ + + + + 5:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + 3:   abnormal cell death [MP:0000313] <5>(29|41) (33|15|5)
+ + 2:   abnormal apoptosis [MP:0001648] <30>(27|38) (30|13|5)
+ + 2:   abnormal embryonic tissue physiology [MP:0008932] <8>(1|3) (1|2|2)
+ 1:   abnormal neural crest cell physiology [MP:0012745] <4>(1|2) (1|2|2)
+ 1:   abnormal embryonic tissue cell apoptosis [MP:0013503] <4>(0|1) (0|0|0)
0:   abnormal neural crest cell apoptosis [MP:0009844] <1>(0|0) (0|0|0)
- 1:   increased neural crest cell apoptosis [MP:0012744] <4>(0|0) (0|0|0)