Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of cardiovascular system electrophysiology (HP:0030956)help
Parent Node:
expand
Arrhythmia (HP:0011675)help
..Starting node
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Bradycardia (HP:0001662)help
Term ID: 1662
Name: Bradycardia
Synonym: Brachycardia; Slow heartbeats
Definition: A slower than normal heart rate (in adults, slower than 60 beats per minute).
Comments:
Reference: HP:0001662
Genes and Diseases:
 
       Child Nodes:
........expandSinus bradycardia (HP:0001688) help

 Sister Nodes: 
..expandAbnormal electrophysiology of sinoatrial node origin (HP:0011702) help
..expandAbnormal heart rate variability (HP:0031860) help
..expandCardiac arrest (HP:0001695) help
..expandPalpitations (HP:0001962) help
..expandSupraventricular arrhythmia (HP:0005115) help
..expandTachycardia (HP:0001649) help
..expandVentricular arrhythmia (HP:0004308) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001662HP:0001662Bradycardia0BRAT1 CL E G H221927614498Rigidity and multifocal seizure syndrome, lethal neonatal614498C3281029OMIM184721701614506
HP:0001662HP:0001662Bradycardia0BRAT1 CL E G H221927614498Rigidity and multifocal seizure syndrome, lethal neonatal614498C3281029OMIM172521701614506
HP:0001662HP:0001662Bradycardia0CACNA1C CL E G H775601005Timothy syndrome601005C1832916OMIM118301390114205
HP:0001662HP:0001662Bradycardia0CACNA1C CL E G H775601005Timothy syndrome601005C1832916OMIM116581390114205
HP:0001662HP:0001662Bradycardia0CACNA1D CL E G H776614896Sinoatrial node dysfunction and deafness614896C3554018OMIM17441391114206
HP:0001662HP:0001662Bradycardia0CACNA1D CL E G H776614896Sinoatrial node dysfunction and deafness614896C3554018OMIM14771391114206
HP:0001662HP:0001662Bradycardia0CACNA2D1 CL E G H78151083ORPHA14451399114204
HP:0001662HP:0001662Bradycardia0CACNA2D1 CL E G H78151083ORPHA13901399114204
HP:0001662HP:0001662Bradycardia0CASQ2 CL E G H845611938Ventricular tachycardia, catecholaminergic polymorphic, 2611938C2677794OMIM14311513114251
HP:0001662HP:0001662Bradycardia0CASQ2 CL E G H845611938Ventricular tachycardia, catecholaminergic polymorphic, 2611938C2677794OMIM13781513114251
HP:0001662HP:0001662Bradycardia0CAVIN1 CL E G H284119613327Lipodystrophy, congenital generalized, type 4613327C2750069OMIM11109688603198
HP:0001662HP:0001662Bradycardia0CAVIN1 CL E G H284119613327Lipodystrophy, congenital generalized, type 4613327C2750069OMIM11099688603198
HP:0001662HP:0001662Bradycardia0COQ9 CL E G H57017614654Coenzyme Q10 deficiency, primary, 5614654C3553374OMIM116425302612837
HP:0001662HP:0001662Bradycardia0COQ9 CL E G H57017614654Coenzyme Q10 deficiency, primary, 5614654C3553374OMIM112725302612837
HP:0001662HP:0001662Bradycardia0DST CL E G H667614653Neuropathy, hereditary sensory and autonomic, type VI614653C3539003OMIM124181090113810
HP:0001662HP:0001662Bradycardia0DST CL E G H667614653Neuropathy, hereditary sensory and autonomic, type VI614653C3539003OMIM119031090113810
HP:0001662HP:0001662Bradycardia0GLUL CL E G H2752610015Glutamine deficiency, congenital610015C1864910OMIM12074341138290
HP:0001662HP:0001662Bradycardia0GLUL CL E G H2752610015Glutamine deficiency, congenital610015C1864910OMIM11924341138290
HP:0001662HP:0001662Bradycardia0GNB5 CL E G H10681617173Intellectual developmental disorder with cardiac arrhythmia617173C4310682OMIM11334401604447
HP:0001662HP:0001662Bradycardia0GNB5 CL E G H10681617173Intellectual developmental disorder with cardiac arrhythmia617173C4310682OMIM11304401604447
HP:0001662HP:0001662Bradycardia0HTRA2 CL E G H274296172483-methylglutaconic aciduria, type VIII617248C4310650OMIM113214348606441
HP:0001662HP:0001662Bradycardia0HTRA2 CL E G H274296172483-methylglutaconic aciduria, type VIII617248C4310650OMIM19614348606441
HP:0001662HP:0001662Bradycardia0KCNH2 CL E G H375751083ORPHA123046251152427
HP:0001662HP:0001662Bradycardia0KCNH2 CL E G H375751083ORPHA121096251152427
HP:0001662HP:0001662Bradycardia0KCNJ2 CL E G H375951083ORPHA14496263600681
HP:0001662HP:0001662Bradycardia0KCNJ2 CL E G H375951083ORPHA14046263600681
HP:0001662HP:0001662Bradycardia0KCNQ1 CL E G H378451083ORPHA115356294607542
HP:0001662HP:0001662Bradycardia0KCNQ1 CL E G H378451083ORPHA114356294607542
HP:0001662HP:0001662Bradycardia0KCNQ1 CL E G H3784609621Short QT syndrome 2609621C1865019OMIM115356294607542
HP:0001662HP:0001662Bradycardia0KCNQ1 CL E G H3784609621Short QT syndrome 2609621C1865019OMIM114356294607542
HP:0001662HP:0001662Bradycardia0LIPT1 CL E G H51601616299Lipoyltransferase 1 deficiency616299C4225379OMIM19029569610284
HP:0001662HP:0001662Bradycardia0LIPT1 CL E G H51601616299Lipoyltransferase 1 deficiency616299C4225379OMIM17329569610284
HP:0001662HP:0001662Bradycardia0LMNA CL E G H4000264ORPHA114866636150330
HP:0001662HP:0001662Bradycardia0LMNA CL E G H4000264ORPHA113476636150330
HP:0001662HP:0001662Bradycardia0NPPA CL E G H4878615745Atrial standstill 2615745C3810401OMIM11517939108780
HP:0001662HP:0001662Bradycardia0NPPA CL E G H4878615745Atrial standstill 2615745C3810401OMIM11247939108780
HP:0001662HP:0001662Bradycardia0PAX8 CL E G H7849218700Thyroid dysgenesis218700C1563716OMIM11918622167415
HP:0001662HP:0001662Bradycardia0PAX8 CL E G H7849218700Thyroid dysgenesis218700C1563716OMIM11878622167415
HP:0001662HP:0001662Bradycardia0PPA2 CL E G H27068617222Sudden cardiac failure, infantile617222C4310664OMIM119328883609988
HP:0001662HP:0001662Bradycardia0PPA2 CL E G H27068617222Sudden cardiac failure, infantile617222C4310664OMIM112928883609988
HP:0001662HP:0001662Bradycardia0PRKAG2 CL E G H51422261740Glycogen storage disease of heart, lethal congenital261740C1849813OMIM18619386602743
HP:0001662HP:0001662Bradycardia0PRKAG2 CL E G H51422261740Glycogen storage disease of heart, lethal congenital261740C1849813OMIM18039386602743
HP:0001662HP:0001662Bradycardia0SCN9A CL E G H6335167400Paroxysmal extreme pain disorder167400C1833661OMIM1170810597603415
HP:0001662HP:0001662Bradycardia0SCN9A CL E G H6335167400Paroxysmal extreme pain disorder167400C1833661OMIM1143810597603415
HP:0001662HP:0001662Bradycardia0SGO1 CL E G H151648616201Chronic atrial and intestinal dysrhythmia616201C4015474OMIM13025088609168
HP:0001662HP:0001662Bradycardia0SGO1 CL E G H151648616201Chronic atrial and intestinal dysrhythmia616201C4015474OMIM12925088609168
HP:0001662HP:0001662Bradycardia0SLC25A20 CL E G H788212138Carnitine acylcarnitine translocase deficiency212138C0342791OMIM11341421613698
HP:0001662HP:0001662Bradycardia0SLC25A20 CL E G H788212138Carnitine acylcarnitine translocase deficiency212138C0342791OMIM11181421613698
HP:0001662HP:0001662Bradycardia0TMEM43 CL E G H79188614302Emery-Dreifuss muscular dystrophy 7, autosomal dominant614302C3553060OMIM165328472612048
HP:0001662HP:0001662Bradycardia0TMEM43 CL E G H79188614302Emery-Dreifuss muscular dystrophy 7, autosomal dominant614302C3553060OMIM158528472612048
HP:0001662HP:0001662Bradycardia0TRPM4 CL E G H54795604559Progressive familial heart block type 1B604559C1970298OMIM180617993606936
HP:0001662HP:0001662Bradycardia0TRPM4 CL E G H54795604559Progressive familial heart block type 1B604559C1970298OMIM164417993606936
HP:0001662HP:0001662Bradycardia0TSPYL1 CL E G H7259608800Sudden infant death with dysgenesis of the testes syndrome608800C1837371OMIM13712382604714
HP:0001662HP:0001662Bradycardia0TSPYL1 CL E G H7259608800Sudden infant death with dysgenesis of the testes syndrome608800C1837371OMIM13512382604714
HP:0001662HP:0001662Bradycardia0USP18 CL E G H11274617397Pseudo-torch syndrome 2617397C4479376OMIM115412616607057
HP:0001662HP:0001662Bradycardia0USP18 CL E G H11274617397Pseudo-torch syndrome 2617397C4479376OMIM115112616607057
HP:0001662HP:0001688Sinus bradycardia1BRAT1 CL E G H221927614498Rigidity and multifocal seizure syndrome, lethal neonatal614498C3281029OMIM184721701614506
HP:0001662HP:0001688Sinus bradycardia1BRAT1 CL E G H221927614498Rigidity and multifocal seizure syndrome, lethal neonatal614498C3281029OMIM172521701614506
HP:0001662HP:0001688Sinus bradycardia1CACNA1C CL E G H775601005Timothy syndrome601005C1832916OMIM118301390114205
HP:0001662HP:0001688Sinus bradycardia1CACNA1C CL E G H775601005Timothy syndrome601005C1832916OMIM116581390114205
HP:0001662HP:0001688Sinus bradycardia1CACNA1D CL E G H776614896Sinoatrial node dysfunction and deafness614896C3554018OMIM17441391114206
HP:0001662HP:0001688Sinus bradycardia1CACNA1D CL E G H776614896Sinoatrial node dysfunction and deafness614896C3554018OMIM14771391114206
HP:0001662HP:0001688Sinus bradycardia1CACNA2D1 CL E G H78151083ORPHA14451399114204
HP:0001662HP:0001688Sinus bradycardia1CACNA2D1 CL E G H78151083ORPHA13901399114204
HP:0001662HP:0001688Sinus bradycardia1CASQ2 CL E G H845611938Ventricular tachycardia, catecholaminergic polymorphic, 2611938C2677794OMIM14311513114251
HP:0001662HP:0001688Sinus bradycardia1CASQ2 CL E G H845611938Ventricular tachycardia, catecholaminergic polymorphic, 2611938C2677794OMIM13781513114251
HP:0001662HP:0001688Sinus bradycardia1CAVIN1 CL E G H284119613327Lipodystrophy, congenital generalized, type 4613327C2750069OMIM11109688603198
HP:0001662HP:0001688Sinus bradycardia1CAVIN1 CL E G H284119613327Lipodystrophy, congenital generalized, type 4613327C2750069OMIM11099688603198
HP:0001662HP:0001688Sinus bradycardia1COQ9 CL E G H57017614654Coenzyme Q10 deficiency, primary, 5614654C3553374OMIM116425302612837
HP:0001662HP:0001688Sinus bradycardia1COQ9 CL E G H57017614654Coenzyme Q10 deficiency, primary, 5614654C3553374OMIM112725302612837
HP:0001662HP:0001688Sinus bradycardia1DST CL E G H667614653Neuropathy, hereditary sensory and autonomic, type VI614653C3539003OMIM124181090113810
HP:0001662HP:0001688Sinus bradycardia1DST CL E G H667614653Neuropathy, hereditary sensory and autonomic, type VI614653C3539003OMIM119031090113810
HP:0001662HP:0001688Sinus bradycardia1GLUL CL E G H2752610015Glutamine deficiency, congenital610015C1864910OMIM12074341138290
HP:0001662HP:0001688Sinus bradycardia1GLUL CL E G H2752610015Glutamine deficiency, congenital610015C1864910OMIM11924341138290
HP:0001662HP:0001688Sinus bradycardia1GNB5 CL E G H10681617173Intellectual developmental disorder with cardiac arrhythmia617173C4310682OMIM11334401604447
HP:0001662HP:0001688Sinus bradycardia1GNB5 CL E G H10681617173Intellectual developmental disorder with cardiac arrhythmia617173C4310682OMIM11304401604447
HP:0001662HP:0001688Sinus bradycardia1HTRA2 CL E G H274296172483-methylglutaconic aciduria, type VIII617248C4310650OMIM113214348606441
HP:0001662HP:0001688Sinus bradycardia1HTRA2 CL E G H274296172483-methylglutaconic aciduria, type VIII617248C4310650OMIM19614348606441
HP:0001662HP:0001688Sinus bradycardia1KCNH2 CL E G H375751083ORPHA123046251152427
HP:0001662HP:0001688Sinus bradycardia1KCNH2 CL E G H375751083ORPHA121096251152427
HP:0001662HP:0001688Sinus bradycardia1KCNJ2 CL E G H375951083ORPHA14496263600681
HP:0001662HP:0001688Sinus bradycardia1KCNJ2 CL E G H375951083ORPHA14046263600681
HP:0001662HP:0001688Sinus bradycardia1KCNQ1 CL E G H378451083ORPHA115356294607542
HP:0001662HP:0001688Sinus bradycardia1KCNQ1 CL E G H378451083ORPHA114356294607542
HP:0001662HP:0001688Sinus bradycardia1KCNQ1 CL E G H3784609621Short QT syndrome 2609621C1865019OMIM115356294607542
HP:0001662HP:0001688Sinus bradycardia1KCNQ1 CL E G H3784609621Short QT syndrome 2609621C1865019OMIM114356294607542
HP:0001662HP:0001688Sinus bradycardia1LIPT1 CL E G H51601616299Lipoyltransferase 1 deficiency616299C4225379OMIM19029569610284
HP:0001662HP:0001688Sinus bradycardia1LIPT1 CL E G H51601616299Lipoyltransferase 1 deficiency616299C4225379OMIM17329569610284
HP:0001662HP:0001688Sinus bradycardia1LMNA CL E G H4000264ORPHA114866636150330
HP:0001662HP:0001688Sinus bradycardia1LMNA CL E G H4000264ORPHA113476636150330
HP:0001662HP:0001688Sinus bradycardia1NPPA CL E G H4878615745Atrial standstill 2615745C3810401OMIM11517939108780
HP:0001662HP:0001688Sinus bradycardia1NPPA CL E G H4878615745Atrial standstill 2615745C3810401OMIM11247939108780
HP:0001662HP:0001688Sinus bradycardia1PAX8 CL E G H7849218700Thyroid dysgenesis218700C1563716OMIM11918622167415
HP:0001662HP:0001688Sinus bradycardia1PAX8 CL E G H7849218700Thyroid dysgenesis218700C1563716OMIM11878622167415
HP:0001662HP:0001688Sinus bradycardia1PPA2 CL E G H27068617222Sudden cardiac failure, infantile617222C4310664OMIM119328883609988
HP:0001662HP:0001688Sinus bradycardia1PPA2 CL E G H27068617222Sudden cardiac failure, infantile617222C4310664OMIM112928883609988
HP:0001662HP:0001688Sinus bradycardia1PRKAG2 CL E G H51422261740Glycogen storage disease of heart, lethal congenital261740C1849813OMIM18619386602743
HP:0001662HP:0001688Sinus bradycardia1PRKAG2 CL E G H51422261740Glycogen storage disease of heart, lethal congenital261740C1849813OMIM18039386602743
HP:0001662HP:0001688Sinus bradycardia1SCN9A CL E G H6335167400Paroxysmal extreme pain disorder167400C1833661OMIM1170810597603415
HP:0001662HP:0001688Sinus bradycardia1SCN9A CL E G H6335167400Paroxysmal extreme pain disorder167400C1833661OMIM1143810597603415
HP:0001662HP:0001688Sinus bradycardia1SGO1 CL E G H151648616201Chronic atrial and intestinal dysrhythmia616201C4015474OMIM13025088609168
HP:0001662HP:0001688Sinus bradycardia1SGO1 CL E G H151648616201Chronic atrial and intestinal dysrhythmia616201C4015474OMIM12925088609168
HP:0001662HP:0001688Sinus bradycardia1SLC25A20 CL E G H788212138Carnitine acylcarnitine translocase deficiency212138C0342791OMIM11341421613698
HP:0001662HP:0001688Sinus bradycardia1SLC25A20 CL E G H788212138Carnitine acylcarnitine translocase deficiency212138C0342791OMIM11181421613698
HP:0001662HP:0001688Sinus bradycardia1TMEM43 CL E G H79188614302Emery-Dreifuss muscular dystrophy 7, autosomal dominant614302C3553060OMIM165328472612048
HP:0001662HP:0001688Sinus bradycardia1TMEM43 CL E G H79188614302Emery-Dreifuss muscular dystrophy 7, autosomal dominant614302C3553060OMIM158528472612048
HP:0001662HP:0001688Sinus bradycardia1TRPM4 CL E G H54795604559Progressive familial heart block type 1B604559C1970298OMIM180617993606936
HP:0001662HP:0001688Sinus bradycardia1TRPM4 CL E G H54795604559Progressive familial heart block type 1B604559C1970298OMIM164417993606936
HP:0001662HP:0001688Sinus bradycardia1TSPYL1 CL E G H7259608800Sudden infant death with dysgenesis of the testes syndrome608800C1837371OMIM13712382604714
HP:0001662HP:0001688Sinus bradycardia1TSPYL1 CL E G H7259608800Sudden infant death with dysgenesis of the testes syndrome608800C1837371OMIM13512382604714
HP:0001662HP:0001688Sinus bradycardia1USP18 CL E G H11274617397Pseudo-torch syndrome 2617397C4479376OMIM115412616607057
HP:0001662HP:0001688Sinus bradycardia1USP18 CL E G H11274617397Pseudo-torch syndrome 2617397C4479376OMIM115112616607057
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001662HP:0001662Bradycardia0AGPAT2 CL E G H10555528Acute myeloblastic leukemia type 3ORPHA0205325603100
HP:0001662HP:0001662Bradycardia0AGPAT2 CL E G H10555528Acute myeloblastic leukemia type 3ORPHA0203325603100
HP:0001662HP:0001662Bradycardia0BSCL2 CL E G H26580528Acute myeloblastic leukemia type 3ORPHA037315832606158
HP:0001662HP:0001662Bradycardia0BSCL2 CL E G H26580528Acute myeloblastic leukemia type 3ORPHA033015832606158
HP:0001662HP:0001662Bradycardia0CALM2 CL E G H805616249Long QT syndrome 15616249C4015695OMIM01121445114182
HP:0001662HP:0001662Bradycardia0CALM2 CL E G H805616249Long QT syndrome 15616249C4015695OMIM01031445114182
HP:0001662HP:0001662Bradycardia0CAV1 CL E G H857528Acute myeloblastic leukemia type 3ORPHA0851527601047
HP:0001662HP:0001662Bradycardia0CAV1 CL E G H857528Acute myeloblastic leukemia type 3ORPHA0811527601047
HP:0001662HP:0001662Bradycardia0CAVIN1 CL E G H284119528Acute myeloblastic leukemia type 3ORPHA01109688603198
HP:0001662HP:0001662Bradycardia0CAVIN1 CL E G H284119528Acute myeloblastic leukemia type 3ORPHA01099688603198
HP:0001662HP:0001662Bradycardia0COQ4 CL E G H51117616276Coenzyme Q10 deficiency, primary, 7616276C4225392OMIM018319693612898
HP:0001662HP:0001662Bradycardia0COQ4 CL E G H51117616276Coenzyme Q10 deficiency, primary, 7616276C4225392OMIM016119693612898
HP:0001662HP:0001662Bradycardia0DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM07032770125660
HP:0001662HP:0001662Bradycardia0DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM06292770125660
HP:0001662HP:0001662Bradycardia0EFEMP2 CL E G H30008614437Autosomal recessive cutis laxa type 1B614437C3280798OMIM02723219604633
HP:0001662HP:0001662Bradycardia0EFEMP2 CL E G H30008614437Autosomal recessive cutis laxa type 1B614437C3280798OMIM02533219604633
HP:0001662HP:0001662Bradycardia0FOS CL E G H2353528Acute myeloblastic leukemia type 3ORPHA0293796164810
HP:0001662HP:0001662Bradycardia0GNB5 CL E G H10681617182Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia617182C4310678OMIM01334401604447
HP:0001662HP:0001662Bradycardia0GNB5 CL E G H10681617182Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia617182C4310678OMIM01304401604447
HP:0001662HP:0001662Bradycardia0MYL4 CL E G H4635617280Atrial fibrillation, familial, 18617280C4310636OMIM01237585160770
HP:0001662HP:0001662Bradycardia0MYL4 CL E G H4635617280Atrial fibrillation, familial, 18617280C4310636OMIM0957585160770
HP:0001662HP:0001662Bradycardia0PPARG CL E G H5468528Acute myeloblastic leukemia type 3ORPHA01249236601487
HP:0001662HP:0001662Bradycardia0PPARG CL E G H5468528Acute myeloblastic leukemia type 3ORPHA01089236601487
HP:0001662HP:0001662Bradycardia0TLL1 CL E G H7092613087Atrial septal defect 6613087C2751315OMIM09411843606742
HP:0001662HP:0001662Bradycardia0TLL1 CL E G H7092613087Atrial septal defect 6613087C2751315OMIM09311843606742
HP:0001662HP:0001662Bradycardia0TWNK CL E G H56652609286Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3609286C1836439OMIM02701160606075
HP:0001662HP:0001662Bradycardia0TWNK CL E G H56652609286Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3609286C1836439OMIM02341160606075
HP:0001662HP:0001688Sinus bradycardia1AGPAT2 CL E G H10555528Acute myeloblastic leukemia type 3ORPHA0205325603100
HP:0001662HP:0001688Sinus bradycardia1AGPAT2 CL E G H10555528Acute myeloblastic leukemia type 3ORPHA0203325603100
HP:0001662HP:0001688Sinus bradycardia1BSCL2 CL E G H26580528Acute myeloblastic leukemia type 3ORPHA037315832606158
HP:0001662HP:0001688Sinus bradycardia1BSCL2 CL E G H26580528Acute myeloblastic leukemia type 3ORPHA033015832606158
HP:0001662HP:0001688Sinus bradycardia1CALM2 CL E G H805616249Long QT syndrome 15616249C4015695OMIM01121445114182
HP:0001662HP:0001688Sinus bradycardia1CALM2 CL E G H805616249Long QT syndrome 15616249C4015695OMIM01031445114182
HP:0001662HP:0001688Sinus bradycardia1CAV1 CL E G H857528Acute myeloblastic leukemia type 3ORPHA0851527601047
HP:0001662HP:0001688Sinus bradycardia1CAV1 CL E G H857528Acute myeloblastic leukemia type 3ORPHA0811527601047
HP:0001662HP:0001688Sinus bradycardia1CAVIN1 CL E G H284119528Acute myeloblastic leukemia type 3ORPHA01109688603198
HP:0001662HP:0001688Sinus bradycardia1CAVIN1 CL E G H284119528Acute myeloblastic leukemia type 3ORPHA01099688603198
HP:0001662HP:0001688Sinus bradycardia1COQ4 CL E G H51117616276Coenzyme Q10 deficiency, primary, 7616276C4225392OMIM018319693612898
HP:0001662HP:0001688Sinus bradycardia1COQ4 CL E G H51117616276Coenzyme Q10 deficiency, primary, 7616276C4225392OMIM016119693612898
HP:0001662HP:0001688Sinus bradycardia1DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM07032770125660
HP:0001662HP:0001688Sinus bradycardia1DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM06292770125660
HP:0001662HP:0001688Sinus bradycardia1EFEMP2 CL E G H30008614437Autosomal recessive cutis laxa type 1B614437C3280798OMIM02723219604633
HP:0001662HP:0001688Sinus bradycardia1EFEMP2 CL E G H30008614437Autosomal recessive cutis laxa type 1B614437C3280798OMIM02533219604633
HP:0001662HP:0001688Sinus bradycardia1FOS CL E G H2353528Acute myeloblastic leukemia type 3ORPHA0293796164810
HP:0001662HP:0001688Sinus bradycardia1GNB5 CL E G H10681617182Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia617182C4310678OMIM01334401604447
HP:0001662HP:0001688Sinus bradycardia1GNB5 CL E G H10681617182Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia617182C4310678OMIM01304401604447
HP:0001662HP:0001688Sinus bradycardia1MYL4 CL E G H4635617280Atrial fibrillation, familial, 18617280C4310636OMIM01237585160770
HP:0001662HP:0001688Sinus bradycardia1MYL4 CL E G H4635617280Atrial fibrillation, familial, 18617280C4310636OMIM0957585160770
HP:0001662HP:0001688Sinus bradycardia1PPARG CL E G H5468528Acute myeloblastic leukemia type 3ORPHA01249236601487
HP:0001662HP:0001688Sinus bradycardia1PPARG CL E G H5468528Acute myeloblastic leukemia type 3ORPHA01089236601487
HP:0001662HP:0001688Sinus bradycardia1TLL1 CL E G H7092613087Atrial septal defect 6613087C2751315OMIM09411843606742
HP:0001662HP:0001688Sinus bradycardia1TLL1 CL E G H7092613087Atrial septal defect 6613087C2751315OMIM09311843606742
HP:0001662HP:0001688Sinus bradycardia1TWNK CL E G H56652609286Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3609286C1836439OMIM02701160606075
HP:0001662HP:0001688Sinus bradycardia1TWNK CL E G H56652609286Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3609286C1836439OMIM02341160606075


Genes (44) :AGPAT2 ANK2 BRAT1 BSCL2 BVES CACNA1C CACNA1D CACNA2D1 CALM2 CASQ2 CAV1 CAV3 CAVIN1 COQ4 COQ9 DES DST EFEMP2 FOS GLUL GNB5 HCN4 HTRA2 KCNH2 KCNJ2 KCNQ1 LIPT1 LMNA MYL4 NPPA PAX8 PPA2 PPARG PRKAG2 SCN5A SCN9A SGO1 SLC25A20 TLL1 TMEM43 TRPM4 TSPYL1 TWNK USP18

Diseases (40) :528 614498 601005 614896 51083 616249 611938 613327 616276 614654 601419 614653 614437 610015 617173 617182 617248 609621 616299 264 617280 615745 218700 617222 261740 167400 616201 212138 613087 614302 604559 608800 609286 617397 600919 616812 611818 163800 600858 608567
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.