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Mammalian Phenotype (MP): abnormal cerebellar granule cell migration

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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:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + 4:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ + 2:   abnormal cell migration [MP:0003091] <14>(13|16) (14|12|6)
+ + 2:   abnormal neuron physiology [MP:0004811] <12>(8|12) (11|7|5)
+ 1:   abnormal neuronal migration [MP:0006009] <2>(2|3) (2|3|1)
0:   abnormal cerebellar granule cell migration [MP:0009977](0|0) (0|0|0)