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Disease Ontology (DO): thalassemia

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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:   genetic disease [DOID:630] <11>(19|28) (22|16|7)
+ + + 3:   monogenic disease [DOID:0050177] <7>(17|25) (19|14|6)
+ + 2:   autosomal genetic disease [DOID:0050739] <8>(17|24) (19|14|6)
+ 1:   autosomal recessive disease [DOID:0050737] <89>(10|11) (10|6|3)
0:   thalassemia [DOID:10241] <2>(1|1) (1|0|0)
- 1:   alpha thalassemia [DOID:1099] <3>(0|0) (0|0|0)
- 1:   beta thalassemia [DOID:12241](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Globin-like0.0000000000007517Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Globins0.0000000000005231Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
Globin-like0.000000000000338Direct


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