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Mammalian Phenotype (MP): abnormal chondrocyte physiology

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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)
+ + + 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 chondrocyte physiology [MP:0009780] <2>(0|0) (0|0|0)
- 1:   abnormal chondrocyte apoptosis [MP:0014102] <2>(0|0) (0|0|0)
- 1:   abnormal chondrocyte proliferation [MP:0014099] <2>(0|0) (0|0|0)