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Mammalian Phenotype (MP): abnormal trabecular 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 trabecular bone morphology [MP:0000130] <6>(8|13) (9|2|0)
0:   abnormal trabecular bone mass [MP:0010871] <2>(0|2) (0|0|0)
- 1:   decreased trabecular bone mass [MP:0010873](0|1) (0|0|0)
- 1:   increased trabecular bone mass [MP:0010872](0|1) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ngr ectodomain-like0.01302Inherited
EGF-type module0.01592Inherited


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