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Mammalian Phenotype (MP): abnormal fetal cardiomyocyte morphology

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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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + 3:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + 2:   abnormal heart morphology [MP:0000266] <22>(27|44) (28|25|19)
+ + 2:   abnormal cardiovascular development [MP:0002925] <10>(16|35) (25|19|9)
+ 1:   abnormal heart development [MP:0000267] <10>(5|11) (6|6|4)
0:   abnormal fetal cardiomyocyte morphology [MP:0008788](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Erythroid transcription factor GATA-10.0000003969Direct


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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)
57716,57716
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 0.0006203Direct