Mammalian Phenotype (MP): abnormal skeletal muscle mechanoreceptor morphology

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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:	nervous system phenotype [MP:0003631] <2>	(98|128)	(113|79|50)
+ + + + 4:	abnormal nervous system morphology [MP:0003632] <17>	(76|104)	(91|64|47)
+ + + + 4:	mammalian phenotype [MP:0000001] <29>
+ + + 3:	muscle phenotype [MP:0005369] <2>	(49|57)	(54|37|28)
+ + + 3:	abnormal somatic nervous system morphology [MP:0002752] <7>	(34|47)	(37|25|14)
+ + 2:	abnormal somatic sensory system morphology [MP:0000959] <4>	(26|38)	(29|19|12)
+ + 2:	abnormal muscle morphology [MP:0002108] <16>	(28|31)	(31|22|21)
+ 1:	abnormal skeletal muscle morphology [MP:0000759] <25>	(15|15)	(16|9|5)
+ 1:	abnormal mechanoreceptor morphology [MP:0000972] <4>	(10|12)	(10|7|5)
0:	abnormal skeletal muscle mechanoreceptor morphology [MP:0000990] <2>	(0|0)	(0|0|0)
- 1:	abnormal muscle spindle morphology [MP:0004069] <4>	(0|0)	(0|0|0)
- 1:	abnormal golgi tendon organ morphology [MP:0000999] <1>	(0|0)	(0|0|0)

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