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Mammalian Phenotype (MP): abnormal bone stiffness

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

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)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ 1:   abnormal skeleton physiology [MP:0001533] <12>(17|20) (18|12|6)
0:   abnormal bone stiffness [MP:0013636] <2>(0|1) (0|0|0)
- 1:   decreased bone stiffness [MP:0013639] <2>(0|0) (0|0|0)
- 1:   increased bone stiffness [MP:0013640] <2>(0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
EGF-type module0.0003494Direct


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