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Mammalian Phenotype (MP): intracranial hemorrhage

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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:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + + 4:   abnormal cardiovascular system physiology [MP:0001544] <24>(39|45) (46|26|17)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   abnormal blood circulation [MP:0002128] <13>(17|22) (20|10|6)
+ + 2:   hemorrhage [MP:0001914] <7>(13|18) (15|10|5)
+ + 2:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ 1:   internal hemorrhage [MP:0001634] <13>(5|6) (6|4|4)
+ 1:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
0:   intracranial hemorrhage [MP:0001915] <4>(0|0) (0|1|0)
- 1:   intracerebral hemorrhage [MP:0001916] <1>(0|0) (0|0|0)
- 1:   brainstem hemorrhage [MP:0006051](0|0) (0|0|0)
- 1:   cerebellum hemorrhage [MP:0006052](0|0) (0|0|0)
- 1:   hypothalamus hemorrhage [MP:0006053](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
  • 0.0001286Direct