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Disease Ontology (DO): hemoglobin D 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)
+ + + + + + + + 8:   disease [DOID:4] <8>
+ + + + + + + 7:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + + + 6:   hematopoietic system disease [DOID:74] <7>(27|29) (27|15|8)
+ + + + + 5:   anemia [DOID:2355] <8>(4|5) (4|2|1)
+ + + + 4:   normocytic anemia [DOID:720] <1>(3|2) (3|2|1)
+ + + 3:   hemolytic anemia [DOID:583] <4>(2|2) (3|2|0)
+ + 2:   congenital hemolytic anemia [DOID:589] <4>(2|1) (2|1|0)
+ 1:   hemoglobinopathy [DOID:2860] <4>(1|1) (1|1|0)
0:   hemoglobin D disease [DOID:5378](0|0) (0|0|0)