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Mammalian Phenotype (MP): abnormal ciliary body morphology

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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:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + + 3:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + 2:   abnormal uvea morphology [MP:0005197] <3>(10|7) (10|5|1)
+ + 2:   abnormal anterior eye segment morphology [MP:0005193] <10>(13|13) (14|4|0)
+ 1:   abnormal anterior uvea morphology [MP:0005194] <3>(7|5) (7|3|0)
0:   abnormal ciliary body morphology [MP:0005099] <7>(0|1) (0|0|0)
- 1:   abnormal ciliary process morphology [MP:0014164] <1>(0|0) (0|0|0)
- 1:   abnormal ciliary body pigmentation [MP:0005101](0|0) (0|0|0)
- 1:   abnormal ciliary epithelium morphology [MP:0014175](0|0) (0|0|0)
- 1:   abnormal ciliary muscle morphology [MP:0014163](0|0) (0|0|0)
- 1:   absent ciliary body [MP:0013742](0|0) (0|0|0)
- 1:   ciliary body coloboma [MP:0010719](0|0) (0|0|0)
- 1:   ciliary body hypoplasia [MP:0013743](0|0) (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 domain0.000002721Direct


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