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Disease Ontology (DO): hereditary Wilms' tumor

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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)
+ + + + + + + 7:   disease [DOID:4] <8>
+ + + + + + 6:   disease of cellular proliferation [DOID:14566] <3>(123|191) (129|118|56)
+ + + + + 5:   cancer [DOID:162] <2>(115|181) (120|113|54)
+ + + + 4:   organ system cancer [DOID:0050686] <14>(66|106) (72|58|31)
+ + + 3:   urinary system cancer [DOID:3996] <4>(7|9) (9|11|7)
+ + 2:   kidney cancer [DOID:263] <8>(6|8) (8|10|7)
+ 1:   nephroblastoma [DOID:2154] <7>(1|1) (2|0|0)
0:   hereditary Wilms' tumor [DOID:5183](1|1) (2|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Nuclear receptor ligand-binding domain0.0003178Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Nuclear receptor ligand-binding domain0.0002063Direct


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)
Nuclear receptor ligand-binding domain0.0001923Direct
Glucocorticoid receptor-like (DNA-binding domain)0.0007102Direct


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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