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Phenotypic Abnormality (PA): Splenic rupture

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|46|25)
+ + + + 4:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + 3:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|13|4)
+ + + 3:   Abnormality of the lymphatic system [HP:0100763] <7>(9|19) (15|8|5)
+ + 2:   Abnormality of the spleen [HP:0001743] <2>(7|14) (9|4|3)
+ 1:   Abnormal spleen morphology [HP:0025408] <11>(7|13) (9|4|3)
0:   Splenic rupture [HP:0012223](2|2) (2|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Fibrinogen C-terminal domain-like0.00000000529Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Fibrinogen C-terminal domain-like0.000000004443Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Fibrinogen C-terminal domain-like0.000000002024Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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