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Mammalian Phenotype (MP): abnormal conjunctiva goblet cell morphology

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + + + 4:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + + 3:   abnormal ocular surface morphology [MP:0013754] <4>(0|1) (2|0|0)
+ + + 3:   abnormal anterior eye segment morphology [MP:0005193] <10>(13|13) (14|4|0)
+ + 2:   abnormal conjunctiva morphology [MP:0001310] <7>(0|0) (0|0|0)
+ 1:   abnormal conjunctival epithelium morphology [MP:0004481] <1>(0|0) (0|0|0)
0:   abnormal conjunctiva goblet cell morphology [MP:0012164] <2>(0|0) (0|0|0)
- 1:   abnormal conjunctiva goblet cell number [MP:0013462] <2>(0|0) (0|0|0)
- 1:   abnormal conjunctiva goblet cell differentiation [MP:0013465](0|0) (0|0|0)