SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Erythrocyte inclusion bodies

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(24|35) (31|16|5)
+ 1:   Abnormal erythrocyte morphology [HP:0001877] <20>(3|6) (4|2|1)
0:   Erythrocyte inclusion bodies [HP:0020080] <3>(1|1) (1|0|0)
- 1:   Heinz bodies [HP:0020082](1|1) (1|0|0)
- 1:   Howell-Jolly bodies [HP:0032550](0|0) (0|0|0)
- 1:   Pappenheimer bodies [HP:0020081](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Globin-like0.00009887Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Globins0.00005126Direct


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)
Globin-like0.00004563Direct


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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