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Mammalian Phenotype (MP): retinal 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)
+ + + + + + 6:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   abnormal cardiovascular system physiology [MP:0001544] <24>(39|45) (46|26|17)
+ + + + 4:   abnormal blood circulation [MP:0002128] <13>(17|22) (20|10|6)
+ + + + 4:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + + 3:   hemorrhage [MP:0001914] <7>(13|18) (15|10|5)
+ + + 3:   abnormal posterior eye segment morphology [MP:0005195] <4>(21|24) (23|14|8)
+ + + 3:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + 2:   abnormal eye physiology [MP:0005253] <25>(8|9) (9|5|2)
+ + 2:   internal hemorrhage [MP:0001634] <13>(5|6) (6|4|4)
+ + 2:   abnormal ocular fundus morphology [MP:0002864] <2>(19|23) (21|14|8)
+ 1:   abnormal retina morphology [MP:0001325] <23>(19|23) (21|14|8)
+ 1:   eye hemorrhage [MP:0006203] <2>(0|0) (0|0|0)
0:   retinal hemorrhage [MP:0006185](0|0) (0|0|0)