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Mammalian Phenotype (MP): cochlear degeneration

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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:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + 3:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ + 2:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
+ 1:   abnormal cochlea morphology [MP:0000031] <15>(12|14) (13|8|5)
0:   cochlear degeneration [MP:0000032] <3>(0|0) (1|0|0)
- 1:   organ of Corti degeneration [MP:0000043](0|0) (0|0|0)
- 1:   spiral ligament degeneration [MP:0004864](0|0) (0|0|0)
- 1:   stria vascularis degeneration [MP:0004363](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Second domain of FERM0.0006289Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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