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Disease Ontology (DO): idiopathic pulmonary fibrosis

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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 anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + + 5:   respiratory system disease [DOID:1579] <4>(29|38) (30|14|7)
+ + + + 4:   lower respiratory tract disease [DOID:0050161] <3>(25|33) (26|13|7)
+ + + 3:   lung disease [DOID:850] <16>(14|18) (15|6|3)
+ + 2:   pneumonia [DOID:552] <8>(0|1) (2|0|1)
+ 1:   idiopathic interstitial pneumonia [DOID:2797] <6>(0|0) (1|0|1)
0:   idiopathic pulmonary fibrosis [DOID:0050156](0|0) (1|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Cytokine0.0007137Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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