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Mammalian Phenotype (MP): skeletal muscle fiber degeneration

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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:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ + + 3:   abnormal muscle morphology [MP:0002108] <16>(28|31) (31|22|21)
+ + 2:   muscle degeneration [MP:0000749] <2>(1|1) (1|0|0)
+ + 2:   abnormal skeletal muscle morphology [MP:0000759] <25>(15|15) (16|9|5)
+ + 2:   abnormal muscle fiber morphology [MP:0004087] <7>(4|6) (5|7|6)
+ 1:   skeletal muscle degeneration [MP:0009415] <1>(0|0) (0|0|0)
+ 1:   abnormal skeletal muscle fiber morphology [MP:0003084] <7>(3|4) (3|2|2)
0:   skeletal muscle fiber degeneration [MP:0009412](0|0) (0|0|0)