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Mammalian Phenotype (MP): abnormal electroretinogram waveform feature

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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 electroretinogram waveform feature [MP:0012029] <5>(0|0) (0|0|0)
- 1:   abnormal ERG implicit time [MP:0012033] <2>(0|0) (0|0|0)
- 1:   abnormal ERG latency [MP:0012032] <2>(0|0) (0|0|0)
- 1:   abnormal a wave shape [MP:0012034] <1>(0|0) (0|0|0)
- 1:   abnormal b-wave shape [MP:0012035] <1>(0|0) (0|0|0)
- 1:   abnormal c wave shape [MP:0012040](0|0) (0|0|0)