Mammalian Phenotype (MP): increased ectoderm 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)
+ + + + + + + 7:	mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:	cellular phenotype [MP:0005384] <6>	(95|116)	(103|56|31)
+ + + + + 5:	abnormal embryo development [MP:0001672] <5>	(9|15)	(11|11|5)
+ + + + + 5:	abnormal cell physiology [MP:0005621] <24>	(77|96)	(84|46|25)
+ + + + 4:	abnormal cell death [MP:0000313] <5>	(29|41)	(33|15|5)
+ + + + 4:	embryo phenotype [MP:0005380] <7>	(40|54)	(46|28|19)
+ + + + 4:	abnormal developmental patterning [MP:0002084] <7>	(7|12)	(9|9|3)
+ + + 3:	abnormal embryonic tissue physiology [MP:0008932] <8>	(1|3)	(1|2|2)
+ + + 3:	increased cell death [MP:0012556] <1>	(16|23)	(18|7|3)
+ + + 3:	abnormal gastrulation [MP:0001695] <5>	(4|7)	(6|4|2)
+ + + 3:	abnormal apoptosis [MP:0001648] <30>	(27|38)	(30|13|5)
+ + 2:	abnormal embryonic tissue cell apoptosis [MP:0013503] <4>	(0|1)	(0|0|0)
+ + 2:	abnormal germ layer development [MP:0001674] <3>	(2|2)	(3|1|1)
+ + 2:	increased apoptosis [MP:0006042] <34>	(16|23)	(18|7|3)
+ 1:	increased embryonic tissue cell apoptosis [MP:0013504] <6>	(0|1)	(0|0|0)
+ 1:	abnormal ectoderm development [MP:0001675] <1>	(0|0)	(0|1|1)
0:	increased ectoderm apoptosis [MP:0003895]	(0|0)	(0|0|0)

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