MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandcardiac rhythm disease (MONDO:0007263)
..Starting node
..expandgenetic cardiac rhythm disease ()

       Child Nodes:
........expandatrial conduction disease ()
........expandatrial heart septal defect 7 ()
........expandatrial standstill ()
........expandautosomal recessive limb-girdle muscular dystrophy type 2X ()
........expandbrachydactyly-long thumb syndrome ()
........expandBrugada syndrome ()
........expandchronic atrial and intestinal dysrhythmia ()
........expandcongenital generalized lipodystrophy type 4 ()
........expandcongenital heart block ()
........expandfamilial atrial fibrillation ()
........expandfamilial long QT syndrome ()
........expandfamilial sick sinus syndrome ()
........expandfirst-degree atrioventricular block ()
........expandheart-hand syndrome type 2 ()
........expandHis bundle tachycardia ()
........expandhistiocytoid cardiomyopathy ()  LSDB  L: 00151;
........expandHolt-Oram syndrome ()
........expandidiopathic ventricular fibrillation, non Brugada type ()
........expandLown-Ganong-Levine syndrome ()
........expandprogressive familial heart block ()
........expandprogressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome ()
........expandrecurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome ()
........expandsecond-degree atrioventricular block ()
........expandshort QT syndrome type 1 ()
........expandsino-auricular heart block ()
........expandsinoatrial node dysfunction and deafness ()
........expandthird-degree atrioventricular block ()
........expandtorsade-de-pointes syndrome with short coupling interval ()
........expandventricular tachycardia, familial ()
........expandX-linked intellectual disability-cardiomegaly-congestive heart failure syndrome ()



 Sister Nodes: 
..expandatrial fibrillation (disease) ()
..expandatrial tachycardia ()
..expandcardiac arrest ()
..expandgenetic cardiac rhythm disease ()
..expandnon-genetic cardiac rhythm disease ()
..expandsudden cardiac arrest ()
..expandventricular fibrillation (disease) ()
..expandventricular tachycardia ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15110
Name:genetic cardiac rhythm disease
Definition:An instance of cardiac rhythm disease that is caused by a modification of the individual's genome.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:genetic cardiac rhythm disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal