SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Omphalocele

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
+ + + 3:   Abnormality of the abdominal wall [HP:0004298] <5>(3|5) (3|4|7)
+ + 2:   Abdominal wall defect [HP:0010866] <4>(2|4) (3|4|7)
+ + 2:   Hernia [HP:0100790] <4>(5|7) (5|5|7)
+ 1:   Hernia of the abdominal wall [HP:0004299] <6>(2|4) (3|4|7)
0:   Omphalocele [HP:0001539](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
CalX-like0.00000926Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
CalX-beta domain0.000003191Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
CalX-like0.000003877Direct


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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