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Mammalian Phenotype (MP): abnormal lipid oxidation

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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>
+ + + 3:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + 2:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + 2:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ 1:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ 1:   abnormal lipid homeostasis [MP:0002118] <9>(25|29) (29|17|10)
0:   abnormal lipid oxidation [MP:0010951] <1>(0|0) (0|0|0)
- 1:   abnormal fatty acid oxidation [MP:0010953] <3>(0|0) (0|0|0)