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Mammalian Phenotype (MP): abnormal bony labyrinth

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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 morphology [MP:0002102] <4>(16|21) (18|14|5)
+ 1:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
0:   abnormal bony labyrinth [MP:0004289] <1>(0|0) (0|0|0)
- 1:   otosclerosis [MP:0004897](0|0) (0|0|0)