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Mammalian Phenotype (MP): abnormal hearing electrophysiology

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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:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + 2:   abnormal ear physiology [MP:0003878] <9>(8|8) (8|3|0)
+ 1:   abnormal hearing physiology [MP:0001963] <5>(8|8) (8|2|0)
0:   abnormal hearing electrophysiology [MP:0006335] <7>(0|4) (0|0|0)
- 1:   abnormal auditory brainstem response [MP:0004738] <3>(0|3) (0|0|0)
- 1:   abnormal cochlear nerve compound action potential [MP:0004415] <3>(0|1) (0|0|0)
- 1:   abnormal endocochlear potential [MP:0002630] <3>(0|0) (0|0|0)
- 1:   abnormal cochlear frequency tuning [MP:0006383] <1>(0|0) (0|0|0)
- 1:   abnormal cochlear potential [MP:0006332] <1>(0|0) (0|0|0)
- 1:   abnormal auditory summating potential [MP:0006388](0|0) (0|0|0)
- 1:   abnormal cochlear nerve fiber response [MP:0006324](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)
Clathrin adaptor core protein0.0002774Direct
Motor proteins0.4088Inherited
Nicotinic receptor ligand binding domain-like0.5291Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.5291Inherited


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