Mammalian Phenotype (MP): abnormal cardiac muscle glycogen level

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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)
+ + + + + + + 7:	mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:	homeostasis/metabolism phenotype [MP:0005376] <7>	(140|174)	(149|96|44)
+ + + + + 5:	abnormal homeostasis [MP:0001764] <27>	(103|129)	(113|73|31)
+ + + + 4:	abnormal glucose homeostasis [MP:0002078] <14>	(15|22)	(17|17|8)
+ + + 3:	muscle phenotype [MP:0005369] <2>	(49|57)	(54|37|28)
+ + + 3:	abnormal glycogen homeostasis [MP:0005438] <2>	(5|3)	(6|3|1)
+ + 2:	abnormal glycogen level [MP:0005437] <5>	(2|3)	(3|2|1)
+ + 2:	abnormal muscle morphology [MP:0002108] <16>	(28|31)	(31|22|21)
+ 1:	abnormal muscle glycogen level [MP:0014068] <2>	(1|0)	(1|0|0)
0:	abnormal cardiac muscle glycogen level [MP:0014070] <2>	(0|0)	(0|0|0)
- 1:	decreased cardiac muscle glycogen level [MP:0014072]	(0|0)	(0|0|0)
- 1:	increased cardiac muscle glycogen level [MP:0014071]	(0|0)	(0|0|0)

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