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Disease Ontology (DO): plasma protein metabolism disease

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ 1:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
0:   plasma protein metabolism disease [DOID:2345] <4>(1|1) (1|0|0)
- 1:   alpha 1-antitrypsin deficiency [DOID:13372](0|0) (0|0|0)
- 1:   macroglobulinemia [DOID:9080](0|0) (0|0|0)
- 1:   monoclonal paraproteinemia [DOID:2346](0|0) (0|0|0)
- 1:   polyclonal hypergammaglobulinemia [DOID:2344](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
TNF-like0.0003003Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
TNF-like0.0001988Direct


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)
TNF-like0.000182Direct


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