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Mammalian Phenotype (MP): abnormal hippocampus development

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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>
+ + + + + 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)
+ + + 3:   abnormal cerebral hemisphere morphology [MP:0008540] <9>(8|12) (10|8|4)
+ + + 3:   abnormal nervous system development [MP:0003861] <9>(19|31) (21|14|10)
+ + + 3:   abnormal brain morphology [MP:0002152] <24>(25|42) (35|24|14)
+ + 2:   abnormal brain development [MP:0000913] <15>(6|12) (7|4|1)
+ + 2:   abnormal temporal lobe morphology [MP:0000801] <4>(7|8) (8|5|2)
+ + 2:   abnormal telencephalon morphology [MP:0000787] <9>(15|22) (19|12|6)
+ + 2:   abnormal limbic system morphology [MP:0004166] <6>(7|8) (9|5|2)
+ + 2:   abnormal forebrain morphology [MP:0000783] <8>(18|26) (24|15|8)
+ 1:   abnormal forebrain development [MP:0003232] <2>(3|5) (3|1|0)
+ 1:   abnormal hippocampus morphology [MP:0000807] <12>(7|8) (8|5|2)
0:   abnormal hippocampus development [MP:0000808](0|0) (0|0|0)