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Disease Ontology (DO): heart conduction 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:   heart conduction disease [DOID:10273] <10>(0|0) (0|0|0)
- 1:   Brugada syndrome [DOID:0050451] <9>(0|0) (0|0|0)
- 1:   catecholaminergic polymorphic ventricular tachycardia [DOID:0060674] <5>(0|0) (0|0|0)
- 1:   atrioventricular block [DOID:0050820] <4>(0|0) (0|0|0)
- 1:   progressive familial heart block [DOID:0111073] <3>(0|0) (0|0|0)
- 1:   atrial fibrillation [DOID:0060224] <1>(0|0) (0|0|0)
- 1:   sinoatrial node disease [DOID:0050824] <1>(0|0) (0|0|0)
- 1:   Wolff-Parkinson-White syndrome [DOID:384](0|0) (0|0|0)
- 1:   left bundle branch hemiblock [DOID:10272](0|0) (0|0|0)
- 1:   right bundle branch block [DOID:13209](0|0) (0|0|0)
- 1:   short QT syndrome [DOID:0050793](0|0) (0|0|0)