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Mammalian Phenotype (MP): abnormal ectoderm development

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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:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + + 4:   abnormal embryo development [MP:0001672] <5>(9|15) (11|11|5)
+ + + 3:   abnormal developmental patterning [MP:0002084] <7>(7|12) (9|9|3)
+ + 2:   abnormal gastrulation [MP:0001695] <5>(4|7) (6|4|2)
+ 1:   abnormal germ layer development [MP:0001674] <3>(2|2) (3|1|1)
0:   abnormal ectoderm development [MP:0001675] <1>(0|0) (0|1|1)
- 1:   increased ectoderm apoptosis [MP:0003895](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)
54236,47031
  • 54236 - Ubiquitin-like
  • 47031 - Second domain of FERM
  • 0.000177Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    54236,47031,50729
  • 54236 - Ubiquitin-like
  • 47031 - Second domain of FERM
  • 50729 - PH domain-like
  • 0.000177Direct