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Mammalian Phenotype (MP): ataxia

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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:   behavior/neurological phenotype [MP:0005386] <1>(38|61) (42|40|24)
+ + + 3:   abnormal behavior [MP:0004924] <19>(37|56) (41|37|22)
+ + + 3:   abnormal voluntary movement [MP:0003491] <8>(12|13) (13|13|8)
+ + 2:   abnormal motor capabilities/coordination/movement [MP:0002066] <6>(19|25) (20|23|17)
+ + 2:   abnormal locomotor behavior [MP:0001392] <2>(8|9) (9|10|4)
+ 1:   abnormal locomotor coordination [MP:0003312] <7>(2|2) (2|1|1)
+ 1:   abnormal motor coordination/ balance [MP:0001516] <12>(1|2) (1|4|4)
0:   ataxia [MP:0001393](0|1) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Phosphotyrosine-binding domain (PTB)0.0009958Direct


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Supra-domain (including individual superfamily)