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Mammalian Phenotype (MP): abnormal eye movement

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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)
+ + + + + 5:   behavior/neurological phenotype [MP:0005386] <1>(38|61) (42|40|24)
+ + + + 4:   abnormal behavior [MP:0004924] <19>(37|56) (41|37|22)
+ + + 3:   abnormal motor capabilities/coordination/movement [MP:0002066] <6>(19|25) (20|23|17)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   abnormal voluntary movement [MP:0003491] <8>(12|13) (13|13|8)
+ + 2:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ 1:   abnormal eye physiology [MP:0005253] <25>(8|9) (9|5|2)
+ 1:   abnormal stationary movement [MP:0001388] <4>(3|2) (3|1|1)
0:   abnormal eye movement [MP:0001389] <7>(0|0) (0|0|0)
- 1:   palsy of the eye [MP:0006157] <2>(0|0) (0|0|0)
- 1:   abnormal visual pursuit [MP:0006156](0|0) (0|0|0)
- 1:   eye abduction [MP:0006154](0|0) (0|0|0)
- 1:   eye adduction [MP:0006155](0|0) (0|0|0)
- 1:   oculomotor apraxia [MP:0006224](0|0) (0|0|0)
- 1:   ophthalmoparesis [MP:0003688](0|0) (0|0|0)
- 1:   ophthalmoplegia [MP:0003689](0|0) (0|0|0)