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Mammalian Phenotype (MP): abnormal cochlear nerve compound action potential

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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:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + 4:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + 3:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ + + 3:   abnormal ear physiology [MP:0003878] <9>(8|8) (8|3|0)
+ + 2:   abnormal nervous system electrophysiology [MP:0002272] <7>(4|8) (7|3|0)
+ + 2:   abnormal hearing physiology [MP:0001963] <5>(8|8) (8|2|0)
+ 1:   abnormal action potential [MP:0005402] <2>(0|1) (0|1|0)
+ 1:   abnormal hearing electrophysiology [MP:0006335] <7>(0|4) (0|0|0)
0:   abnormal cochlear nerve compound action potential [MP:0004415] <3>(0|1) (0|0|0)
- 1:   absent cochlear nerve compound action potential [MP:0004416](0|0) (0|0|0)
- 1:   decreased cochlear nerve compound action potential [MP:0004417](0|0) (0|0|0)
- 1:   increased cochlear nerve compound action potential [MP:0004767](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Motor proteins0.0009838Direct


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