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Mammalian Phenotype (MP): delayed endochondral bone ossification

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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 physiology [MP:0001533] <12>(17|20) (18|12|6)
+ + 2:   abnormal bone ossification [MP:0008271] <10>(8|11) (8|1|2)
+ 1:   delayed bone ossification [MP:0000060] <2>(1|1) (1|0|0)
+ 1:   abnormal endochondral bone ossification [MP:0008272] <4>(1|1) (1|0|0)
0:   delayed endochondral bone ossification [MP:0003419](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
FnI-like domain0.00003589Direct


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)
FnI-like domain0.00001662Direct


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