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Mammalian Phenotype (MP): abnormal vision

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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)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ 1:   abnormal eye physiology [MP:0005253] <25>(8|9) (9|5|2)
0:   abnormal vision [MP:0002090] <8>(0|0) (0|0|0)
- 1:   blindness [MP:0002001] <4>(0|0) (0|0|0)
- 1:   abnormal visual acuity [MP:0011832] <1>(0|0) (0|0|0)
- 1:   myopia [MP:0003100] <1>(0|0) (0|0|0)
- 1:   abnormal visual contrast sensitivity [MP:0011831](0|0) (0|0|0)
- 1:   double vision [MP:0006150](0|0) (0|0|0)
- 1:   hemeralopia [MP:0008145](0|0) (0|0|0)
- 1:   hypermetropia [MP:0006153](0|0) (0|0|0)
- 1:   tunnel vision [MP:0006152](0|0) (0|0|0)