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Disease Ontology (DO): hemolytic anemia

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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:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + 3:   hematopoietic system disease [DOID:74] <7>(27|29) (27|15|8)
+ + 2:   anemia [DOID:2355] <8>(4|5) (4|2|1)
+ 1:   normocytic anemia [DOID:720] <1>(3|2) (3|2|1)
0:   hemolytic anemia [DOID:583] <4>(2|2) (3|2|0)
- 1:   congenital hemolytic anemia [DOID:589] <4>(2|1) (2|1|0)
- 1:   hemoglobinuria [DOID:582] <1>(0|0) (0|0|0)
- 1:   Rh deficiency syndrome [DOID:0050641](0|0) (0|0|0)
- 1:   hemolytic-uremic syndrome [DOID:12554](0|1) (1|1|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Thioredoxin-like1Inherited
GST C-terminal domain-like1Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Complement control module/SCR domain1Inherited
Glutathione S-transferase (GST), C-terminal domain1Inherited


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)
Thioredoxin-like1Inherited
Complement control module/SCR domain1Inherited
GST C-terminal domain-like1Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52833,47616
  • 52833 - Thioredoxin-like
  • 47616 - GST C-terminal domain-like
  • 1Inherited
    57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 1Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)