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Mammalian Phenotype (MP): abnormal compact bone mass

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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:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + + 3:   abnormal skeleton morphology [MP:0005508] <15>(41|59) (47|38|25)
+ + 2:   abnormal bone structure [MP:0003795] <17>(17|23) (22|14|6)
+ 1:   abnormal compact bone morphology [MP:0003797] <6>(6|5) (7|1|0)
0:   abnormal compact bone mass [MP:0010960] <2>(1|1) (1|0|0)
- 1:   decreased compact bone mass [MP:0010962](1|1) (1|0|0)
- 1:   increased compact bone mass [MP:0010961](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
L domain-like0.0107Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ngr ectodomain-like0.003069Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
L domain-like0.006711Inherited


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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