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Mammalian Phenotype (MP): abnormal ossification involved in bone remodeling

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + 2:   abnormal skeleton physiology [MP:0001533] <12>(17|20) (18|12|6)
+ 1:   abnormal bone remodeling [MP:0002998] <4>(3|6) (4|4|3)
+ 1:   abnormal bone ossification [MP:0008271] <10>(8|11) (8|1|2)
0:   abnormal ossification involved in bone remodeling [MP:0011720](0|0) (0|0|0)