SUPERFAMILY 1.75 HMM library and genome assignments server

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Disease Ontology (DO): congenital heart 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:   heart disease [DOID:114] <8>(8|11) (9|5|4)
0:   congenital heart disease [DOID:1682] <7>(0|1) (0|0|0)
- 1:   heart septal defect [DOID:1681] <3>(0|0) (0|0|0)
- 1:   dextro-looped transposition of the great arteries [DOID:0060770] <2>(0|0) (0|0|0)
- 1:   patent ductus arteriosus [DOID:13832] <1>(0|0) (0|0|0)
- 1:   dextrocardia [DOID:9565](0|0) (0|0|0)
- 1:   hypoplastic left heart syndrome [DOID:9955](0|0) (0|0|0)
- 1:   scimitar syndrome [DOID:4297](0|0) (0|0|0)
- 1:   tetralogy of Fallot [DOID:6419](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
T-box0.0000002173Direct


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