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Mammalian Phenotype (MP): abnormal cochlear hair cell physiology

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + 4:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ + + 3:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + 3:   abnormal neuron physiology [MP:0004811] <12>(8|12) (11|7|5)
+ + + 3:   abnormal somatic nervous system physiology [MP:0005423] <3>(0|0) (0|1|0)
+ + 2:   abnormal sensory neuron physiology [MP:0010055] <5>(0|0) (0|1|0)
+ + 2:   abnormal ear physiology [MP:0003878] <9>(8|8) (8|3|0)
+ 1:   abnormal hair cell physiology [MP:0003879] <3>(0|0) (0|1|0)
0:   abnormal cochlear hair cell physiology [MP:0004432] <2>(0|0) (0|0|0)
- 1:   abnormal cochlear outer hair cell physiology [MP:0004434] <2>(0|0) (0|0|0)
- 1:   abnormal cochlear inner hair cell physiology [MP:0004433](0|0) (0|0|0)