Mammalian Phenotype (MP): abnormal cardiac cell glucose uptake

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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)
+ + + + 4:	cellular phenotype [MP:0005384] <6>	(95|116)	(103|56|31)
+ + + 3:	muscle phenotype [MP:0005369] <2>	(49|57)	(54|37|28)
+ + + 3:	abnormal cell physiology [MP:0005621] <24>	(77|96)	(84|46|25)
+ + + 3:	mammalian phenotype [MP:0000001] <29>
+ + 2:	abnormal cellular glucose import [MP:0003925] <3>	(1|1)	(1|1|0)
+ + 2:	cardiovascular system phenotype [MP:0005385] <2>	(67|85)	(77|57|35)
+ + 2:	abnormal muscle physiology [MP:0002106] <23>	(25|33)	(27|16|11)
+ 1:	abnormal cardiovascular system physiology [MP:0001544] <24>	(39|45)	(46|26|17)
+ 1:	abnormal muscle cell glucose uptake [MP:0004130] <1>	(1|1)	(1|0|0)
0:	abnormal cardiac cell glucose uptake [MP:0004039]	(0|0)	(0|0|0)

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