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Mammalian Phenotype (MP): abnormal eyelid development

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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>
+ + + 3:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + 2:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ 1:   abnormal eyelid morphology [MP:0001340] <21>(4|8) (6|5|1)
+ 1:   abnormal eye development [MP:0001286] <22>(6|5) (6|2|2)
0:   abnormal eyelid development [MP:0009651] <1>(0|0) (0|0|0)
- 1:   abnormal eyelid fusion [MP:0009263] <2>(0|0) (0|0|0)