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Disease Ontology (DO): hemoglobinuria

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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)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   hematopoietic system disease [DOID:74] <7>(27|29) (27|15|8)
+ + + + 4:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + 3:   urinary system disease [DOID:18] <10>(20|29) (22|11|6)
+ + + 3:   anemia [DOID:2355] <8>(4|5) (4|2|1)
+ + 2:   normocytic anemia [DOID:720] <1>(3|2) (3|2|1)
+ + 2:   kidney disease [DOID:557] <24>(19|28) (21|11|6)
+ 1:   proteinuria [DOID:576] <1>(3|4) (3|1|0)
+ 1:   hemolytic anemia [DOID:583] <4>(2|2) (3|2|0)
0:   hemoglobinuria [DOID:582] <1>(0|0) (0|0|0)
- 1:   paroxysmal nocturnal hemoglobinuria [DOID:0060284](0|0) (0|0|0)