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Mammalian Phenotype (MP): abnormal periocular mesenchyme 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)
+ + + + 4:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   growth/size/body region phenotype [MP:0005378] <12>(64|95) (71|47|27)
+ + + 3:   abnormal embryo morphology [MP:0014134] <4>(23|31) (26|14|12)
+ + + 3:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + + 3:   abnormal head morphology [MP:0000432] <8>(12|23) (14|5|2)
+ + 2:   abnormal embryonic tissue morphology [MP:0002085] <35>(17|21) (19|10|9)
+ + 2:   abnormal head development [MP:0012176] <2>(1|1) (1|0|0)
+ + 2:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ 1:   abnormal head mesenchyme morphology [MP:0011260] <10>(1|1) (1|0|0)
+ 1:   abnormal eye development [MP:0001286] <22>(6|5) (6|2|2)
0:   abnormal periocular mesenchyme morphology [MP:0004054](0|0) (0|0|0)