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Disease Ontology (DO): peripheral vascular 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)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + 2:   cardiovascular system disease [DOID:1287] <3>(41|53) (41|24|14)
+ 1:   vascular disease [DOID:178] <13>(37|48) (38|22|11)
0:   peripheral vascular disease [DOID:341] <8>(0|1) (0|1|0)
- 1:   retinal vascular occlusion [DOID:1729] <3>(0|0) (0|0|0)
- 1:   Raynaud disease [DOID:10300](0|0) (0|0|0)
- 1:   diabetic angiopathy [DOID:11713](0|0) (0|0|0)
- 1:   erythromelalgia [DOID:9240](0|0) (0|0|0)
- 1:   mesenteric vascular occlusion [DOID:13252](0|0) (0|0|0)
- 1:   priapism [DOID:9286](0|0) (0|0|0)
- 1:   telangiectasis [DOID:1272](0|1) (0|1|0)
- 1:   thromboangiitis obliterans [DOID:12918](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Phoshoinositide 3-kinase (PI3K), catalytic domain0.0000006398Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.00004775Direct