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Mammalian Phenotype (MP): decreased total retina thickness

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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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + + + + 5:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + + + 4:   abnormal posterior eye segment morphology [MP:0005195] <4>(21|24) (23|14|8)
+ + + 3:   abnormal ocular fundus morphology [MP:0002864] <2>(19|23) (21|14|8)
+ + 2:   abnormal retina morphology [MP:0001325] <23>(19|23) (21|14|8)
+ 1:   abnormal total retina thickness [MP:0011963] <2>(0|0) (0|0|1)
0:   decreased total retina thickness [MP:0011965](0|0) (0|0|1)


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

Supra-domain (including individual superfamily)

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0001115Direct