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Mammalian Phenotype (MP): conductive hearing loss

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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:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + + 4:   abnormal ear physiology [MP:0003878] <9>(8|8) (8|3|0)
+ + + 3:   abnormal hearing physiology [MP:0001963] <5>(8|8) (8|2|0)
+ + 2:   impaired hearing [MP:0006325] <7>(5|4) (5|2|0)
+ 1:   conductive hearing impairment [MP:0006326] <1>(1|1) (1|0|0)
0:   conductive hearing loss [MP:0004739](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain-like0.00001029Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.000004728Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Homeodomain-like0.00000453Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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