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Mammalian Phenotype (MP): decreased motor neuron number

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + 3:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + 3:   abnormal spinal cord morphology [MP:0000955] <13>(7|9) (8|4|3)
+ + 2:   abnormal neuron morphology [MP:0002882] <29>(36|59) (40|26|19)
+ + 2:   abnormal neuron number [MP:0008946] <3>(8|16) (9|9|8)
+ + 2:   abnormal spinal cord grey matter morphology [MP:0008503] <4>(1|1) (1|0|1)
+ 1:   abnormal motor neuron morphology [MP:0000937] <4>(1|1) (1|0|0)
+ 1:   decreased neuron number [MP:0008948] <8>(6|11) (6|5|4)
0:   decreased motor neuron number [MP:0000939](0|0) (0|0|0)