Mammalian Phenotype (MP): myoclonus

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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)
+ + + + 4:	nervous system phenotype [MP:0003631] <2>	(98|128)	(113|79|50)
+ + + + 4:	behavior/neurological phenotype [MP:0005386] <1>	(38|61)	(42|40|24)
+ + + 3:	abnormal behavior [MP:0004924] <19>	(37|56)	(41|37|22)
+ + + 3:	abnormal muscle physiology [MP:0002106] <23>	(25|33)	(27|16|11)
+ + + 3:	abnormal nervous system physiology [MP:0003633] <38>	(43|60)	(52|31|18)
+ + 2:	seizures [MP:0002064] <6>	(10|15)	(13|3|0)
+ + 2:	muscle twitch [MP:0009046] <1>	(2|2)	(2|1|0)
+ 1:	convulsive seizures [MP:0000947] <5>	(3|4)	(3|2|0)
+ 1:	muscle spasm [MP:0000743] <4>	(1|2)	(1|1|0)
0:	myoclonus [MP:0000243]	(0|0)	(0|0|0)

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