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Mammalian Phenotype (MP): abnormal Bergmann glial cell morphology

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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)
+ + + + + + + + + + 10:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + + + 9:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + + + + + 8:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + + + + + 7:   abnormal brain morphology [MP:0002152] <24>(25|42) (35|24|14)
+ + + + + + 6:   abnormal hindbrain morphology [MP:0000841] <7>(6|9) (7|12|7)
+ + + + + 5:   abnormal metencephalon morphology [MP:0000847] <3>(6|9) (7|12|7)
+ + + + 4:   abnormal cerebellum morphology [MP:0000849] <7>(6|8) (6|12|6)
+ + + 3:   abnormal cerebellar cortex morphology [MP:0004097] <8>(5|6) (5|9|5)
+ + 2:   abnormal cerebellar layer morphology [MP:0009956] <3>(4|4) (4|6|3)
+ 1:   abnormal cerebellar Purkinje cell layer [MP:0000875] <4>(1|1) (1|1|0)
0:   abnormal Bergmann glial cell morphology [MP:0010387] <2>(0|0) (0|1|0)
- 1:   abnormal Bergmann glial cell differentiation [MP:0010388](0|0) (0|0|0)
- 1:   ectopic Bergmann glia cells [MP:0002763](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0005423Direct