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Mammalian Phenotype (MP): absent organ of Corti

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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)
+ + + + + + + + 8:   mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + + + 5:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ + + + 4:   abnormal membranous labyrinth morphology [MP:0000035] <2>(11|14) (12|9|5)
+ + + + 4:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
+ + + 3:   abnormal cochlea morphology [MP:0000031] <15>(12|14) (13|8|5)
+ + + 3:   abnormal cochlear labyrinth morphology [MP:0004426] <1>(10|12) (11|8|5)
+ + 2:   abnormal scala media morphology [MP:0003169] <9>(10|12) (11|8|5)
+ 1:   abnormal organ of Corti morphology [MP:0000042] <7>(10|12) (10|7|5)
0:   absent organ of Corti [MP:0000044](0|0) (0|0|0)