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Mammalian Phenotype (MP): absent corpus callosum

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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)
+ + + + + + + + 8:   mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + + 5:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + + + 5:   abnormal brain morphology [MP:0002152] <24>(25|42) (35|24|14)
+ + + + 4:   abnormal brain white matter morphology [MP:0008026] <6>(3|9) (5|4|3)
+ + + + 4:   abnormal nervous system tract morphology [MP:0000778] <8>(5|10) (7|5|4)
+ + + + 4:   abnormal forebrain morphology [MP:0000783] <8>(18|26) (24|15|8)
+ + + 3:   abnormal brain commissure morphology [MP:0002199] <3>(1|7) (3|4|3)
+ + + 3:   abnormal telencephalon morphology [MP:0000787] <9>(15|22) (19|12|6)
+ + 2:   abnormal cerebral hemisphere morphology [MP:0008540] <9>(8|12) (10|8|4)
+ + 2:   abnormal dorsal telencephalic commissure morphology [MP:0008219] <2>(0|4) (0|1|0)
+ 1:   abnormal corpus callosum morphology [MP:0000780] <3>(0|3) (0|1|0)
0:   absent corpus callosum [MP:0002196](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)0.00004753Direct


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