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Mammalian Phenotype (MP): abnormal fetal cardiomyocyte proliferation

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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)
+ + + 3:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + 2:   abnormal cardiovascular system physiology [MP:0001544] <24>(39|45) (46|26|17)
+ + 2:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ + 2:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ 1:   abnormal cell proliferation [MP:0000350] <31>(15|19) (18|11|5)
+ 1:   abnormal fetal cardiomyocyte physiology [MP:0011390] <2>(0|1) (0|0|0)
+ 1:   abnormal muscle physiology [MP:0002106] <23>(25|33) (27|16|11)
0:   abnormal fetal cardiomyocyte proliferation [MP:0003567] <2>(0|1) (0|0|0)
- 1:   decreased fetal cardiomyocyte proliferation [MP:0011395](0|0) (0|0|0)
- 1:   increased fetal cardiomyocyte proliferation [MP:0011394](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Erythroid transcription factor GATA-10.00003198Direct


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