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Mammalian Phenotype (MP): corneal vascularization

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + + 4:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + + 3:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + + 3:   abnormal cardiovascular system physiology [MP:0001544] <24>(39|45) (46|26|17)
+ + 2:   abnormal anterior eye segment morphology [MP:0005193] <10>(13|13) (14|4|0)
+ + 2:   abnormal blood vessel physiology [MP:0000249] <11>(13|17) (15|5|3)
+ 1:   abnormal cornea morphology [MP:0001312] <18>(4|7) (5|2|0)
+ 1:   pathological neovascularization [MP:0003711] <4>(6|9) (7|4|1)
0:   corneal vascularization [MP:0005542](0|1) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Forkhead DNA-binding domain0.0008717Direct


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