| Hypertension, Essential |
|
Elevated mean arterial pressure, Elevated diastolic blood pressure, Elevated systolic blood pressure |
OMIM:145500 |
| Cardiac Conduction Defect |
|
Arrhythmia, Syncope |
OMIM:115080 |
| Hyperaldosteronism, Familial, Type Iv |
|
Hypertension |
OMIM:617027 |
| His Bundle Tachycardia |
|
Junctional ectopic tachycardia, Arrhythmia, Cardiomyopathy |
ORPHA:3283 |
| Catecholaminergic Polymorphic Ventricular Tachycardia |
|
Sudden cardiac death, Syncope, Ventricular tachycardia |
ORPHA:3286 |
| Supravalvular Aortic Stenosis |
|
Supravalvular aortic stenosis, Arrhythmia |
ORPHA:3193 |
| Coronary Artery Disease, Autosomal Dominant, 1 |
|
Myocardial infarction, Hypertension |
OMIM:608320 |
| Long Qt Syndrome 13 |
|
Paroxysmal atrial fibrillation, Atrial fibrillation, Hypertension, Pulmonary embolism, Atrioventr... |
OMIM:613485 |
| Ventricular Fibrillation, Paroxysmal Familial, 1 |
|
Ventricular fibrillation, Tachycardia, Syncope |
OMIM:603829 |
| Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 |
|
Syncope, Cardiac arrest, Ventricular tachycardia |
OMIM:614916 |
| Intracranial Hypertension, Idiopathic |
|
Hypertension |
OMIM:243200 |
| Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy |
|
Atrial standstill, Abnormal left ventricular function, Atrial fibrillation, Ventricular tachycard... |
OMIM:604772 |
| Abdominal Obesity-Metabolic Syndrome 1 |
|
Hypertension |
OMIM:605552 |
| Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
|
Hypertension |
OMIM:605572 |
| Cardiomyopathy, Familial Hypertrophic, 11 |
|
Arrhythmia, Hypertrophic cardiomyopathy |
OMIM:612098 |
| Congenital Pulmonary Veins Atresia Or Stenosis |
|
Hypertension |
ORPHA:3188 |
| Cataract 46, Juvenile-Onset, With Or Without Arrhythmic Cardiomyopathy |
|
Sudden cardiac death, Arrhythmia |
OMIM:212500 |
| Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 |
|
Syncope, Bradycardia, Ventricular tachycardia |
OMIM:611938 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 |
|
Ventricular arrhythmia, Prolonged QRS complex, T-wave inversion, Ventricular tachycardia, Right v... |
OMIM:611528 |
| Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 |
|
Syncope, Prolonged QT interval, Ventricular tachycardia |
OMIM:614021 |
| Brugada Syndrome |
|
Ventricular arrhythmia, Sick sinus syndrome, Ventricular fibrillation, Supraventricular tachycard... |
ORPHA:130 |
| Cardiomyopathy, Dilated, 1O |
|
Dilated cardiomyopathy, Impaired myocardial contractility, Ventricular tachycardia |
OMIM:608569 |
| Atrial Fibrillation, Familial, 1 |
|
Tachycardia, Atrial fibrillation |
OMIM:608583 |
| Atrial Fibrillation, Familial, 3 |
|
Tachycardia, Atrial fibrillation |
OMIM:607554 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 |
|
Palpitations, Prolonged QRS complex, Ventricular extrasystoles, Ventricular tachycardia, Sudden c... |
OMIM:604400 |
| Cardiomyopathy, Familial Hypertrophic, 12 |
|
Paroxysmal atrial fibrillation, Sudden cardiac death, Cardiomyopathy, Ventricular tachycardia |
OMIM:612124 |
| Ventricular Tachycardia, Familial |
|
Sudden cardiac death, Right bundle branch block, Paroxysmal ventricular tachycardia |
OMIM:192605 |
| Cardiac Arrhythmia Syndrome, With Or Without Skeletal Muscle Weakness |
|
Ventricular extrasystoles, Ventricular tachycardia, Cardiac arrest, Shock, Polymorphic ventricula... |
OMIM:615441 |
| Incessant Infant Ventricular Tachycardia |
|
Bundle branch block, Prolonged QRS complex, Wolff-Parkinson-White syndrome, Ventricular tachycard... |
ORPHA:45453 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 |
|
Palpitations, Ventricular extrasystoles, Ventricular tachycardia, Sudden cardiac death, Right ven... |
OMIM:610193 |
| Trimethylaminuria |
|
Tachycardia, Hypertension |
OMIM:602079 |
| Brugada Syndrome 1 |
|
Supraventricular tachycardia with an accessory connection mediated pathway, Atrial flutter, Atria... |
OMIM:601144 |
| Atrial Fibrillation, Familial, 18 |
|
Paroxysmal atrial fibrillation, Palpitations, Bradycardia, Permanent atrial fibrillation |
OMIM:617280 |
| Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy |
|
Paroxysmal supraventricular tachycardia, Atrial flutter, Ventricular extrasystoles, Atrial fibril... |
OMIM:616117 |
| Cardiomyopathy, Dilated, 1G |
|
Premature atrial contractions, Reduced ejection fraction, Atrial fibrillation, Ventricular tachyc... |
OMIM:604145 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 |
|
Ventricular extrasystoles, Ventricular tachycardia, Sudden cardiac death, Ventricular fibrillatio... |
OMIM:607450 |
| Short Qt Syndrome 3 |
|
Shortened QT interval, Palpitations, Tachycardia |
OMIM:609622 |
| Cardiomyopathy, Dilated, 1E |
|
Palpitations, Premature atrial contractions, Atrial standstill, Atrial flutter, Ventricular extra... |
OMIM:601154 |
| Sinoatrial Node Dysfunction And Deafness |
|
Bradycardia |
OMIM:614896 |
| Cardiomyopathy, Dilated, 1Y |
|
Dilated cardiomyopathy, Mitral regurgitation, Congestive heart failure, Ventricular tachycardia |
OMIM:611878 |
| Hydroxykynureninuria |
|
Hypotension, Tachycardia |
OMIM:236800 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 14 |
|
Palpitations, Ventricular extrasystoles, Ventricular tachycardia, Left bundle branch block, Presy... |
OMIM:618920 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 |
|
Bundle branch block, Ventricular tachycardia |
OMIM:615616 |
| Paragangliomas 6 |
|
Hypertension |
OMIM:618464 |
| Congenital Heart Defects, Multiple Types, 3 |
|
Atrial fibrillation, Atrioventricular block, Tachycardia, Atrioventricular dissociation, Right bu... |
OMIM:614954 |
| Brugada Syndrome 8 |
|
Right bundle branch block, ST segment elevation, Ventricular tachycardia |
OMIM:613123 |
| Osteochondrodysplasia, Rhizomelic, With Callosal Agenesis, Thrombocytopenia, Hydrocephalus, And Hypertension |
|
Hypertension |
OMIM:166990 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 |
|
Ventricular arrhythmia, Sudden cardiac death, Right ventricular cardiomyopathy |
OMIM:107970 |
| Cardiomyopathy, Familial Hypertrophic, 16 |
|
Left bundle branch block, Asymmetric septal hypertrophy, Atrial fibrillation, Ventricular tachyca... |
OMIM:613838 |
| Nathalie Syndrome |
|
Arrhythmia |
ORPHA:2663 |
| Hyperaldosteronism, Familial, Type Ii |
|
Hypertension |
OMIM:605635 |
| Variegate Porphyria |
|
Tachycardia |
OMIM:176200 |
| Atrial Fibrillation, Familial, 14 |
|
Paroxysmal atrial fibrillation, ST segment elevation, Prolonged PR interval, Hypertension |
OMIM:615378 |
| Cardiomyopathy, Dilated, 1P |
|
Ventricular arrhythmia, Congestive heart failure, Dilated cardiomyopathy, Reduced systolic function |
OMIM:609909 |
| Paroxysmal Extreme Pain Disorder |
|
Tachycardia, Bradycardia |
OMIM:167400 |
| Heart-Hand Syndrome, Slovenian Type |
|
Arrhythmia, Abnormal electrophysiology of sinoatrial node origin, Supraventricular arrhythmia, Ab... |
ORPHA:168796 |
| Cardiomyopathy, Familial Hypertrophic, 10 |
|
Palpitations, Asymmetric septal hypertrophy, T-wave inversion, Ventricular tachycardia, Sudden ca... |
OMIM:608758 |
| Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia |
|
Arrhythmia, Sick sinus syndrome, Bradycardia |
OMIM:617182 |
| Idiopathic Neonatal Atrial Flutter |
|
Reduced ejection fraction, Arrhythmia, Paroxysmal supraventricular tachycardia, Abnormal left ven... |
ORPHA:45452 |
| Wolff-Parkinson-White Syndrome |
|
Palpitations, Prolonged QRS complex, Paroxysmal supraventricular tachycardia, Wolff-Parkinson-Whi... |
OMIM:194200 |
| Long-Thumb Brachydactyly Syndrome |
|
Arrhythmia |
OMIM:112430 |
| Long Qt Syndrome 15 |
|
Ventricular fibrillation, Prolonged QT interval, Cardiac arrest, Bradycardia, Prolonged QTc interval |
OMIM:616249 |
| Cardiomyopathy, Familial Hypertrophic, 17 |
|
Palpitations, Cardiomyopathy, Ventricular tachycardia |
OMIM:613873 |
| Familial Short Qt Syndrome |
|
Ventricular arrhythmia, Palpitations, Shortened QT interval, Atrial fibrillation, Sudden cardiac ... |
ORPHA:51083 |
| Brugada Syndrome 9 |
|
Palpitations, Presyncope, ST segment elevation |
OMIM:616399 |
| Short Qt Syndrome 2 |
|
Shortened QT interval, Atrial fibrillation, Sudden cardiac death, Ventricular fibrillation, Brady... |
OMIM:609621 |
| Atrial Fibrillation, Familial, 4 |
|
Palpitations, Premature atrial contractions, Paroxysmal atrial fibrillation, Atrial fibrillation,... |
OMIM:611493 |
| Melorheostosis With Osteopoikilosis |
|
Hypertension |
ORPHA:1879 |
| Atrial Septal Defect 6 |
|
Atrial fibrillation, Bradycardia |
OMIM:613087 |
| Cardiac Arrhythmia, Ankyrin-B-Related |
|
Atrial fibrillation, Sudden cardiac death, Sinus bradycardia, Prolonged QT interval, Syncope |
OMIM:600919 |
| Progressive Familial Heart Block, Type Ii |
|
Sudden cardiac death, Complete heart block with narrow QRS complexes, Atrioventricular block, Sin... |
OMIM:140400 |
| Brachydactyly-Arterial Hypertension Syndrome |
|
Hypertension |
ORPHA:1276 |
| Corticosteroid-Binding Globulin Deficiency |
|
Hypotension, Hypertension |
OMIM:611489 |
| Acute Peripheral Arterial Occlusion |
|
Abnormal capillary physiology, Myocardial infarction, Supraventricular tachycardia, Abnormality o... |
ORPHA:90064 |
| Ventricular Extrasystoles With Syncope, Perodactyly, And Robin Sequence |
|
Ventricular extrasystoles, Tachycardia, Syncope |
OMIM:192445 |
| Progressive Familial Heart Block, Type Ib |
|
Arrhythmia, Atrioventricular block, Shortened PR interval, Prolonged QT interval, Left anterior f... |
OMIM:604559 |
| Atrial Standstill |
|
Palpitations, Reduced ejection fraction, Arrhythmia, Ischemic stroke, Cardiac conduction abnormal... |
ORPHA:1344 |
| Atrial Septal Defect, Sinus Venosus Type |
|
Premature atrial contractions, Palpitations, Cardiac conduction abnormality, Supraventricular arr... |
ORPHA:99105 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 |
|
Ventricular arrhythmia, Palpitations, Sudden cardiac death, Right ventricular cardiomyopathy, Syn... |
OMIM:610476 |
| Cardiomyopathy, Dilated, 1Aa, With Or Without Left Ventricular Noncompaction |
|
Atrial fibrillation, Atrioventricular block, Supraventricular tachycardia, Cardiac arrest, Dilate... |
OMIM:612158 |
| Atrial Septal Defect-Atrioventricular Conduction Defects Syndrome |
|
Arrhythmia, Bundle branch block |
ORPHA:1479 |
| Intellectual Developmental Disorder With Cardiac Arrhythmia |
|
Arrhythmia, Sick sinus syndrome, Bradycardia |
OMIM:617173 |
| Hyperthyroidism, Familial Gestational |
|
Tachycardia |
OMIM:603373 |
| Coronary Artery Disease, Autosomal Dominant 2 |
|
Sudden cardiac death, Myocardial infarction, Hypertension |
OMIM:610947 |
| Arterial Calcification, Generalized, Of Infancy, 2 |
|
Myocardial infarction, Congestive heart failure, Hypertension |
OMIM:614473 |
| Cardiomyopathy-Cataract-Hip Spine Disease Syndrome |
|
Arrhythmia, Hypertension, Pulmonary embolism, Congestive heart failure, Hypertrophic cardiomyopathy |
ORPHA:1345 |
| Nail-Patella-Like Renal Disease |
|
Hypertension |
ORPHA:2613 |
| Hypertension And Brachydactyly Syndrome |
|
Hypertension |
OMIM:112410 |
| Spastic Paraplegia-Nephritis-Deafness Syndrome |
|
Hypertension |
ORPHA:2820 |
| Coproporphyria, Hereditary |
|
Tachycardia, Hypertension |
OMIM:121300 |
| Jervell And Lange-Nielsen Syndrome 1 |
|
Sudden cardiac death, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:220400 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 |
|
Ventricular arrhythmia, Right ventricular cardiomyopathy, T-wave inversion in the right precordia... |
OMIM:602086 |
| Cardiomyopathy, Dilated, 1B |
|
Ventricular arrhythmia, Impaired myocardial contractility, Congestive heart failure, Dilated card... |
OMIM:600884 |
| Short Qt Syndrome 1 |
|
Palpitations, Paroxysmal atrial fibrillation, Shortened QT interval, Sudden cardiac death, Cardia... |
OMIM:609620 |
| Liddle Syndrome 3 |
|
Hypertension |
OMIM:618126 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 |
|
Ventricular arrhythmia, Right ventricular cardiomyopathy, T-wave inversion in the right precordia... |
OMIM:602087 |
| Atrial Fibrillation, Familial, 10 |
|
Paroxysmal atrial fibrillation, Paroxysmal atrial tachycardia, Atrial flutter, Tricuspid regurgit... |
OMIM:614022 |
| Cardiomyopathy, Dilated, 1Dd |
|
Dilated cardiomyopathy, Sudden cardiac death, Congestive heart failure |
OMIM:613172 |
| Preeclampsia/Eclampsia 1 |
|
Hypertension |
OMIM:189800 |
| Metachromatic Leukodystrophy, Adult-Onset, With Normal Arylsulfatase A |
|
Hypotension |
OMIM:156310 |
| Long Qt Syndrome 3 |
|
Sudden cardiac death, Ventricular fibrillation, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:603830 |
| Long Qt Syndrome 2 |
|
Sudden cardiac death, Ventricular fibrillation, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:613688 |
| Long Qt Syndrome 6 |
|
Sudden cardiac death, Ventricular fibrillation, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:613693 |
| Long Qt Syndrome 5 |
|
Sudden cardiac death, Ventricular fibrillation, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:613695 |
| Cardiomyopathy, Familial Hypertrophic, 1 |
|
Asymmetric septal hypertrophy, Arrhythmia, Congestive heart failure |
OMIM:192600 |
| Atrial Standstill 1 |
|
Premature atrial contractions, Atrial standstill, Atrial cardiomyopathy, Paroxysmal atrial fibril... |
OMIM:108770 |
| Long Qt Syndrome 1 |
|
Sudden cardiac death, Ventricular fibrillation, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:192500 |
| Familial Dilated Cardiomyopathy With Conduction Defect Due To Lmna Mutation |
|
Ventricular arrhythmia, Cardiac conduction abnormality, Atrial flutter, Abnormal left ventricular... |
ORPHA:300751 |
| Pheochromocytoma--Islet Cell Tumor Syndrome |
|
Positive regitine blocking test, Episodic hypertension, Cerebral hemorrhage, Tachycardia, Congest... |
OMIM:171420 |
| Focal Segmental Glomerulosclerosis 5 |
|
Hypertension |
OMIM:613237 |
| Long Qt Syndrome 9 |
|
Ventricular arrhythmia, Prolonged QT interval, Sinus bradycardia, Cardiac arrest |
OMIM:611818 |
| Familial Progressive Cardiac Conduction Defect |
|
Arrhythmia, Bundle branch block, Congestive heart failure, Heart block, Syncope |
ORPHA:871 |
| Iga Nephropathy, Susceptibility To, 3 |
|
Hypertension |
OMIM:616818 |
| Cystic Hamartoma Of Lung And Kidney |
|
Hypertension |
ORPHA:2111 |
| Atrial Tachyarrhythmia With Short Pr Interval |
|
Paroxysmal atrial fibrillation, Paroxysmal atrial tachycardia, Shortened PR interval, Permanent a... |
OMIM:108950 |
| Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency |
|
Supraventricular tachycardia, Cardiomyopathy |
OMIM:255100 |
| Focal Segmental Glomerulosclerosis 3, Susceptibility To |
|
Hypertension |
OMIM:607832 |
| Long Qt Syndrome 16 |
|
Second degree atrioventricular block, Prolonged QTc interval, Bradycardia, T-wave alternans |
OMIM:618782 |
| Liddle Syndrome |
|
Arrhythmia, Cerebral ischemia, Hypertension |
ORPHA:526 |
| Chronic Atrial And Intestinal Dysrhythmia |
|
Atrial flutter, Sick sinus syndrome, Atrial fibrillation, Pulmonic stenosis, Mitral regurgitation... |
OMIM:616201 |
| Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant |
|
Arrhythmia, Atrial fibrillation, Bradycardia |
OMIM:614302 |
| Focal Segmental Glomerulosclerosis 2 |
|
Hypertension |
OMIM:603965 |
| Malignant Hyperthermia, Susceptibility To, 5 |
|
Tachycardia |
OMIM:601887 |
| Iga Nephropathy, Susceptibility To, 2 |
|
Hypertension |
OMIM:613944 |
| Long Qt Syndrome 12 |
|
Ventricular fibrillation, Prolonged QTc interval, Torsade de pointes, Syncope |
OMIM:612955 |
| Ventricular Arrythmias Due To Cardiac Ryanodine Receptor Calcium Release Deficiency Syndrome |
|
Polymorphic and polytopic ventricular extrasystoles, Sudden cardiac death, Ventricular fibrillati... |
OMIM:115000 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 |
|
Ventricular arrhythmia, Effort-induced polymorphic ventricular tachycardia, Right ventricular car... |
OMIM:600996 |
| Long Qt Syndrome 14 |
|
Atrioventricular block, Ventricular fibrillation, Sinus bradycardia, Prolonged QT interval, Cardi... |
OMIM:616247 |
| Deafness, Nerve Type, With Mesenteric Diverticula Of Small Bowel And Progressive Sensory Neuropathy |
|
Tachycardia |
OMIM:221400 |
| Brugada Syndrome 3 |
|
Ventricular arrhythmia, Shortened QT interval, J wave, Atrial fibrillation, Sudden cardiac death,... |
OMIM:611875 |
| Sick Sinus Syndrome 1 |
|
Sick sinus syndrome, Ventricular escape rhythm, Atrioventricular block, Absent P wave, Sinus brad... |
OMIM:608567 |
| Left Ventricular Noncompaction 8 |
|
Arrhythmia, Abnormal left ventricular function, Congestive heart failure, Dilated cardiomyopathy,... |
OMIM:615373 |
| Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma |
|
Dilated cardiomyopathy, Congestive heart failure, Ventricular tachycardia |
OMIM:605676 |
| Glycogen Storage Disease Xv |
|
Ventricular arrhythmia, Right bundle branch block |
OMIM:613507 |
| Renal Failure, Progressive, With Hypertension |
|
Hypertension |
OMIM:161900 |
| Jervell And Lange-Nielsen Syndrome 2 |
|
Sudden cardiac death, Prolonged QT interval, Torsade de pointes, Syncope |
OMIM:612347 |
| Paragangliomas 3 |
|
Palpitations, Tachycardia, Hypertension associated with pheochromocytoma |
OMIM:605373 |
| Hypertension, Early-Onset, Autosomal Dominant, With Severe Exacerbation In Pregnancy |
|
Hypertension |
OMIM:605115 |
| Infant Acute Respiratory Distress Syndrome |
|
Hypotension, Tachycardia, Cardiac arrest, Bradycardia |
ORPHA:70587 |
| Congenital Tricuspid Stenosis |
|
Hypotension, Tricuspid regurgitation, Tricuspid stenosis, Heart murmur, Congestive heart failure,... |
ORPHA:95459 |
| Thyrotoxic Periodic Paralysis, Susceptibility To, 2 |
|
Palpitations, Tachycardia |
OMIM:613239 |
| Naxos Disease |
|
Arrhythmia, Sudden cardiac death, Congestive heart failure, Paroxysmal ventricular tachycardia, C... |
ORPHA:34217 |
| Cardiomyopathy, Dilated, 1A |
|
Ventricular arrhythmia, Atrial flutter, Atrial fibrillation, Congestive heart failure, Dilated ca... |
OMIM:115200 |
| Moyamoya Disease With Early-Onset Achalasia |
|
Raynaud phenomenon, Hypertension |
ORPHA:401945 |
| Cardiomyopathy, Dilated, 1Nn |
|
Dilated cardiomyopathy, Mitral regurgitation, Ventricular arrhythmia |
OMIM:615916 |
| Peripartum Cardiomyopathy |
|
Cardiogenic shock, Palpitations, Reduced ejection fraction, Right ventricular failure, Dilated ca... |
ORPHA:563 |
| Thyrotoxic Periodic Paralysis, Susceptibility To, 1 |
|
Palpitations, Tachycardia |
OMIM:188580 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 |
|
Sudden cardiac death, Ventricular extrasystoles, Right ventricular cardiomyopathy |
OMIM:604401 |
| Brugada Syndrome 6 |
|
Ventricular fibrillation, Cardiac arrest, ST segment elevation |
OMIM:613119 |
| Malignant Hyperthermia, Susceptibility To, 1 |
|
Hypotension, Tachycardia |
OMIM:145600 |
| Angiomatosis, Diffuse Corticomeningeal, Of Divry And Van Bogaert |
|
Telangiectases producing 'marbled' skin, Hypertension |
OMIM:206570 |
| Tako-Tsubo Cardiomyopathy |
|
Ventricular arrhythmia, Cardiogenic shock, Palpitations, Arrhythmia, Decreased QRS voltage, Angin... |
ORPHA:66529 |
| Cardiomyopathy, Familial Hypertrophic, 6 |
|
Asymmetric septal hypertrophy, Ventricular preexcitation, Wolff-Parkinson-White syndrome, Atrial ... |
OMIM:600858 |
| Cardiomyopathy, Dilated, 1C, With Or Without Left Ventricular Noncompaction |
|
Ventricular arrhythmia, Sudden cardiac death, Congestive heart failure, Dilated cardiomyopathy |
OMIM:601493 |
| Moyamoya Disease 6 With Or Without Achalasia |
|
Ischemic stroke, Raynaud phenomenon, Hypertension |
OMIM:615750 |
| Lipodystrophy, Familial Partial, Type 4 |
|
Hypertension |
OMIM:613877 |
| Sudden Cardiac Failure, Infantile |
|
Congestive heart failure, Bradycardia, Hypertrophic cardiomyopathy, Myocarditis |
OMIM:617222 |
| Phosphoribosylpyrophosphate Synthetase Superactivity |
|
Cardiomyopathy, Arrhythmia, Hypertension |
ORPHA:3222 |
| Muscular Dystrophy, Progressive Pectorodorsal |
|
Arrhythmia |
OMIM:310095 |
| Long Qt Syndrome 10 |
|
Atrial fibrillation, Sudden cardiac death, Atrioventricular block, Prolonged QT interval, T-wave ... |
OMIM:611819 |
| Muscular Dystrophy, Becker Type |
|
Abnormal EKG, Arrhythmia, Cardiomyopathy |
OMIM:300376 |
| Hyperinsulinism Due To Ucp2 Deficiency |
|
Palpitations, Tachycardia, Hypertrophic cardiomyopathy, Syncope |
ORPHA:276556 |
| Paragangliomas 1 |
|
Palpitations, Tachycardia, Hypertension associated with pheochromocytoma |
OMIM:168000 |
| Ventricular Fibrillation, Paroxysmal Familial, 2 |
|
Sudden cardiac death, Ventricular fibrillation, Ventricular extrasystoles |
OMIM:612956 |
| Glomerulopathy With Fibronectin Deposits 1 |
|
Hypertension |
OMIM:137950 |
| Glycogen Storage Disease With Severe Cardiomyopathy Due To Glycogenin Deficiency |
|
Palpitations, Arrhythmia, T-wave inversion, Ventricular tachycardia, Ventricular fibrillation, ST... |
ORPHA:263297 |
| Atrial Fibrillation, Familial, 7 |
|
Paroxysmal atrial fibrillation, Palpitations, Prolonged PR interval, Prolonged QTc interval |
OMIM:612240 |
| Brugada Syndrome 2 |
|
Sudden cardiac death, Ventricular fibrillation, Prolonged PR interval, First degree atrioventricu... |
OMIM:611777 |
| Morbid Obesity And Spermatogenic Failure |
|
Myocardial infarction, Congestive heart failure, Hypertension |
OMIM:615703 |
| Cardiomyopathy, Dilated, 1R |
|
Ventricular arrhythmia, Restrictive cardiomyopathy, Congestive heart failure, Dilated cardiomyopathy |
OMIM:613424 |
| Multiple Mitochondrial Dysfunctions Syndrome 1 |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:605711 |
| Lessel-Kubisch Syndrome |
|
Hypertension |
OMIM:618681 |
| Cardiomyopathy, Familial Hypertrophic, 21 |
|
Arrhythmia, Cardiomyopathy |
OMIM:614676 |
| Drug-Induced Autoimmune Hemolytic Anemia |
|
Congestive heart failure, Tachycardia |
ORPHA:90037 |
| Maternally-Inherited Diabetes And Deafness |
|
Arrhythmia, Congestive heart failure, Hypertension, Hypertrophic cardiomyopathy |
ORPHA:225 |
| Hydroxykynureninuria |
|
Hypotension, Tachycardia |
ORPHA:79155 |
| Atrial Fibrillation, Familial, 15 |
|
Atrial flutter, Atrial fibrillation |
OMIM:615770 |
| Iga Nephropathy, Susceptibility To, 1 |
|
Hypertension |
OMIM:161950 |
| Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction |
|
Tachycardia, Hypertension |
OMIM:613870 |
| Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency |
|
Palpitations, Tachycardia, Hypertrophic cardiomyopathy, Syncope |
ORPHA:276575 |
| Pseudohypoaldosteronism, Type Iia |
|
Hypertension |
OMIM:145260 |
| Rowley-Rosenberg Syndrome |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:268500 |
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
Arrhythmia, Wolff-Parkinson-White syndrome, Abnormal left ventricular function, Hypertension, Con... |
OMIM:540000 |
| Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency |
|
Palpitations, Tachycardia, Hypertrophic cardiomyopathy, Syncope |
ORPHA:276580 |
| Hydrops, Lactic Acidosis, And Sideroblastic Anemia |
|
Arrhythmia, Hypertension |
OMIM:617021 |
| Snakebite Envenomation |
|
Cardiogenic shock, Intracranial hemorrhage, Hypotension, Epistaxis, Myocardial infarction, Tachyc... |
ORPHA:449285 |
| Cardiomyopathy, Familial Hypertrophic, 8 |
|
Palpitations, Restrictive cardiomyopathy, T-wave inversion, Sudden cardiac death, Ventricular fib... |
OMIM:608751 |
| Cirrhosis, Familial |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:215600 |
| Arterial Calcification, Generalized, Of Infancy, 1 |
|
Myocardial infarction, Congestive heart failure, Hypertension |
OMIM:208000 |
| Familial Cervical Artery Dissection |
|
Recurrent cerebral hemorrhage, Subarachnoid hemorrhage, Hypertension, Cerebral ischemia, Transien... |
ORPHA:36382 |
| Romano-Ward Syndrome |
|
Ventricular arrhythmia, Torsade de pointes, Sudden cardiac death, Abnormal T-wave, Sinus bradycar... |
ORPHA:101016 |
| Acquired Methemoglobinemia |
|
Palpitations, Arrhythmia, Tachycardia, Syncope |
ORPHA:464453 |
| Grange Syndrome |
|
Hypertension, Aortic regurgitation |
ORPHA:79094 |
| Focal Segmental Glomerulosclerosis 1 |
|
Hypertension |
OMIM:603278 |
| Cardiomyopathy, Dilated, 2B |
|
Dilated cardiomyopathy, Congestive heart failure, Atrial fibrillation |
OMIM:614672 |
| Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome |
|
Tachycardia |
ORPHA:276608 |
| Cardiomyopathy, Dilated, With Woolly Hair, Keratoderma, And Tooth Agenesis |
|
Dilated cardiomyopathy, Tachycardia, Syncope |
OMIM:615821 |
| Congenital Left Ventricular Aneurysm |
|
Abnormal T-wave, Arrhythmia, Congestive heart failure, Abnormal ST segment |
ORPHA:1055 |
| Obesity Due To Melanocortin 4 Receptor Deficiency |
|
Hypertension |
ORPHA:71529 |
| Carnitine-Acylcarnitine Translocase Deficiency |
|
Hypotension, Ventricular extrasystoles, Ventricular tachycardia, Atrioventricular block, Cardiac ... |
OMIM:212138 |
| Sinus Node Disease And Myopia |
|
Abnormal electrophysiology of sinoatrial node origin, Sick sinus syndrome |
OMIM:182190 |
| Myopathy, Myofibrillar, 1 |
|
Restrictive cardiomyopathy, Third degree atrioventricular block, Dilated cardiomyopathy, Bradycar... |
OMIM:601419 |
| Hyperinsulinism Due To Hnf1A Deficiency |
|
Palpitations, Tachycardia, Syncope |
ORPHA:324575 |
| Pheochromocytoma |
|
Positive regitine blocking test, Episodic hypertension, Cerebral hemorrhage, Tachycardia, Congest... |
OMIM:171300 |
| Obesity Due To Sim1 Deficiency |
|
Hypotension, Postural hypotension with compensatory tachycardia |
ORPHA:369873 |
| Familial Dilated Cardiomyopathy |
|
Ventricular arrhythmia, Palpitations, Reduced ejection fraction, Arrhythmia, Elevated pulmonary a... |
ORPHA:217607 |
| Glucocorticoid Resistance, Generalized |
|
Hypertension |
OMIM:615962 |
| Naxos Disease |
|
Ventricular arrhythmia, Palpitations, Prolonged QRS complex, T-wave inversion, Ventricular extras... |
OMIM:601214 |
| Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
|
Hypertension |
OMIM:600666 |
| Linear Skin Defects With Multiple Congenital Anomalies 3 |
|
Dilated cardiomyopathy, Ventricular fibrillation, Cardiac arrest, Ventricular tachycardia |
OMIM:300952 |
| Inflammatory Skin And Bowel Disease, Neonatal, 2 |
|
Hypertension |
OMIM:616069 |
| Sneddon Syndrome |
|
Cerebral hemorrhage, Ischemic stroke, Hypertension |
OMIM:182410 |
| Mercury Poisoning |
|
Hypotension, Tachycardia, Hypertension |
ORPHA:330021 |
| Glomerulopathy With Fibronectin Deposits 2 |
|
Hypertension |
OMIM:601894 |
| Denys-Drash Syndrome |
|
Hypertension |
ORPHA:220 |
| Liddle Syndrome 2 |
|
Hypertension |
OMIM:618114 |
| Fibronectin Glomerulopathy |
|
Cerebral hemorrhage, Hypertension |
ORPHA:84090 |
| Cardiogenic Shock |
|
Low pulse pressure, Right ventricular failure, Hypotension, Abnormal left ventricular function, I... |
ORPHA:97292 |
| Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 |
|
Ventricular arrhythmia, Palpitations, Sudden cardiac death, Right ventricular cardiomyopathy, Syn... |
OMIM:609040 |
| Tetanus |
|
Tachycardia, Hypertension, Bradycardia |
ORPHA:3299 |
| Primary Membranoproliferative Glomerulonephritis |
|
Myocardial infarction, Hypertension |
ORPHA:54370 |
| Atrial Septal Defect, Ostium Secundum Type |
|
Palpitations, Arrhythmia, Bundle branch block, Right ventricular failure, Supraventricular arrhyt... |
ORPHA:99103 |
| Hyperaldosteronism, Familial, Type I |
|
Hypertension |
OMIM:103900 |
| Sick Sinus Syndrome 2 |
|
Aortic regurgitation, Sick sinus syndrome, Atrial fibrillation, Ventricular fibrillation, Sinus b... |
OMIM:163800 |
| X-Linked Intellectual Disability-Plagiocephaly Syndrome |
|
Bradycardia |
ORPHA:2898 |
| Postorgasmic Illness Syndrome |
|
Palpitations, Hypertension |
ORPHA:279947 |
| Complete Atrioventricular Septal Defect |
|
Right ventricular failure, Elevated pulmonary artery pressure, Third heart sound, Abnormal atriov... |
ORPHA:1329 |
| Brugada Syndrome 4 |
|
Shortened QT interval, Atrial fibrillation, Syncope |
OMIM:611876 |
| Brugada Syndrome 7 |
|
Atrial flutter, ST segment elevation |
OMIM:613120 |
| Car T Cell Therapy-Associated Cytokine Release Syndrome |
|
Reduced ejection fraction, Arrhythmia, Hypotension, Tachycardia, Heart block, Capillary leak |
ORPHA:542323 |
| Atrial Standstill 2 |
|
Palpitations, Atrial standstill, Atrial cardiomyopathy, Atrial arrhythmia, Absent P wave, Bradyca... |
OMIM:615745 |
| Hyperthyroidism, Nonautoimmune |
|
Tachycardia |
OMIM:609152 |
| Erythrocytosis, Familial, 1 |
|
Myocardial infarction, Cerebral hemorrhage, Hypertension |
OMIM:133100 |
| Pseudohypoaldosteronism Type 2 |
|
Hypertension |
ORPHA:757 |
| Myotonic Dystrophy 2 |
|
Palpitations, Tachycardia |
OMIM:602668 |
| Preeclampsia |
|
Elevated diastolic blood pressure, Hypertension, Elevated systolic blood pressure |
ORPHA:275555 |
| Amyloidosis, Familial Visceral |
|
Hypertension |
OMIM:105200 |
| Pseudohypoaldosteronism, Type Iib |
|
Hypertension |
OMIM:614491 |
| Pseudohypoaldosteronism, Type Iid |
|
Hypertension |
OMIM:614495 |
| Familial Partial Lipodystrophy, Köbberling Type |
|
Hypertension |
ORPHA:79084 |
| Glutaric Aciduria Iii |
|
Hypertension |
OMIM:231690 |
| Jervell And Lange-Nielsen Syndrome |
|
Arrhythmia, Ventricular fibrillation, Prolonged QTc interval, Torsade de pointes, Syncope |
ORPHA:90647 |
| Polycystic Kidney Disease 6 With Or Without Polycystic Liver Disease |
|
Hypertension |
OMIM:618061 |
| Atrial Fibrillation, Familial, 11 |
|
Atrial fibrillation |
OMIM:614049 |
| Atrial Fibrillation, Familial, 6 |
|
Atrial fibrillation |
OMIM:612201 |
| Atrial Fibrillation, Familial, 5 |
|
Atrial fibrillation |
OMIM:611494 |
| Pulmonary Hypertension, Primary, 1 |
|
Right ventricular failure, Increased pulmonary vascular resistance, Hypertension, Pulmonary arter... |
OMIM:178600 |
| Pulmonary Hypertension, Primary, 4 |
|
Pulmonary arterial hypertension, Increased pulmonary vascular resistance, Arrhythmia, Elevated pu... |
OMIM:615344 |
| Coenzyme Q10 Deficiency, Primary, 7 |
|
Bradycardia, Hypertrophic cardiomyopathy |
OMIM:616276 |
| Senior-Loken Syndrome |
|
Hypertension |
ORPHA:3156 |
| Autoimmune Hemolytic Anemia, Warm Type |
|
Congestive heart failure, Tachycardia |
ORPHA:90033 |
| Perry Syndrome |
|
Hypotension |
ORPHA:178509 |
| Stiff-Person Syndrome |
|
Tachycardia, Hypertension |
OMIM:184850 |
| Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease |
|
Mitral regurgitation, Hypertension |
OMIM:173900 |
| Atrioventricular Septal Defect 3 |
|
Midsystolic murmur, Hypertension, Congestive heart failure, First degree atrioventricular block, ... |
OMIM:600309 |
| Methanol Poisoning |
|
Intracranial hemorrhage, Inflammatory arteriopathy, Hypertension, Permanent atrial fibrillation, ... |
ORPHA:31825 |
| Aapoaiv Amyloidosis |
|
Cardiac conduction abnormality, Abnormal cardiac ventricular function, Atrial flutter, Atrial fib... |
ORPHA:439232 |
| Sneddon Syndrome |
|
Intracranial hemorrhage, Hypertension |
ORPHA:820 |
| Abdominal Obesity-Metabolic Syndrome 3 |
|
Myocardial infarction, Hypertension |
OMIM:615812 |
| Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency |
|
Hypertension |
OMIM:201910 |
| Carnitine Palmitoyltransferase Ii Deficiency, Infantile |
|
Dilated cardiomyopathy, Ventricular tachycardia |
OMIM:600649 |
| Mixed-Type Autoimmune Hemolytic Anemia |
|
Tachycardia |
ORPHA:90036 |
| Adrenal Hyperplasia, Congenital, Due To 17-Alpha-Hydroxylase Deficiency |
|
Hypertension |
OMIM:202110 |
| Brugada Syndrome 5 |
|
Ventricular fibrillation, Bundle branch block, ST segment elevation |
OMIM:612838 |
| Congenital Disorder Of Glycosylation, Type It |
|
Sudden cardiac death, Aborted sudden cardiac death, Tachycardia, Dilated cardiomyopathy |
OMIM:614921 |
| Chromosome 17Q23.1-Q23.2 Deletion Syndrome |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:613355 |
| Porphyria, Acute Intermittent |
|
Tachycardia, Hypertension |
OMIM:176000 |
| Paragangliomas 4 |
|
Palpitations, Tachycardia, Hypertension associated with pheochromocytoma |
OMIM:115310 |
| Hereditary Pulmonary Alveolar Proteinosis |
|
Tachycardia |
ORPHA:264675 |
| Potocki-Shaffer Syndrome |
|
Hypertension |
ORPHA:52022 |
| Multicentric Carpotarsal Osteolysis Syndrome |
|
Hypertension |
OMIM:166300 |
| Glycogen Storage Disease Of Heart, Lethal Congenital |
|
Hypotension, Congestive heart failure, Shortened PR interval, Bradycardia, Cardiomyopathy |
OMIM:261740 |
| Serotonin Syndrome |
|
Hypotension, Tachycardia, Hypertension |
ORPHA:43116 |
| Carney Triad |
|
Hypertension, Arrhythmia, Tachycardia, Gastrointestinal hemorrhage |
ORPHA:139411 |
| Analbuminemia |
|
Hypotension |
OMIM:616000 |
| Pseudohypoaldosteronism, Type Iic |
|
Hypertension |
OMIM:614492 |
| Pseudohypoaldosteronism, Type Iie |
|
Hypertension |
OMIM:614496 |
| Takayasu Arteritis |
|
Hypertensive crisis, Hypertension, Myocardial infarction, Cerebral ischemia, Pulmonary arterial h... |
ORPHA:3287 |
| X-Linked Hypohidrotic Ectodermal Dysplasia |
|
Hypertension |
ORPHA:181 |
| Plin1-Related Familial Partial Lipodystrophy |
|
Hypertension |
ORPHA:280356 |
| Thiamine-Responsive Megaloblastic Anemia Syndrome |
|
Paroxysmal atrial tachycardia, Congestive heart failure, Cardiac arrest |
ORPHA:49827 |
| Histiocytoid Cardiomyopathy |
|
Wolff-Parkinson-White syndrome, Atrial flutter, Atrial fibrillation, Ventricular tachycardia, Atr... |
ORPHA:137675 |
| Lcat Deficiency |
|
Hypertension |
ORPHA:650 |
| Glycogen Storage Disease Due To Muscle Glycogen Phosphorylase Deficiency |
|
Tachycardia, Hypertrophic cardiomyopathy |
ORPHA:368 |
| Juvenile Neuronal Ceroid Lipofuscinosis |
|
Tachycardia |
ORPHA:79264 |
| Relapsing Fever |
|
Hypotension, Tachycardia, Epistaxis |
ORPHA:91547 |
| Very Long Chain Acyl-Coa Dehydrogenase Deficiency |
|
Arrhythmia, Ventricular tachycardia, Atrioventricular block, Ventricular fibrillation, Tachycardi... |
ORPHA:26793 |
| Chromosome 5Q12 Deletion Syndrome |
|
Hypotension |
OMIM:615668 |
| Idiopathic Non-Lupus Full-House Nephropathy |
|
Hypertension |
ORPHA:567544 |
| Cutis Marmorata Telangiectatica Congenita |
|
Telangiectasia, Hypertension |
OMIM:219250 |
| Gnb5-Related Intellectual Disability-Cardiac Arrhythmia Syndrome |
|
Arrhythmia, Sick sinus syndrome, Ventricular escape rhythm, Prolonged PR interval, Bradycardia |
ORPHA:542306 |
| Mitochondrial Dna-Related Cardiomyopathy And Hearing Loss |
|
Dilated cardiomyopathy, Congestive heart failure, Hypertension, Hypertrophic cardiomyopathy |
ORPHA:1349 |
| Neuropathy, Hereditary Sensory And Autonomic, Type Vi |
|
Tachycardia, Bradycardia |
OMIM:614653 |
| Lipoyltransferase 1 Deficiency |
|
Pulmonary arterial hypertension, Bradycardia |
OMIM:616299 |
| Chromosome 1P36.33 Duplication Syndrome, Atad3 Gene Cluster, Autosomal Dominant |
|
Dilated cardiomyopathy, Bradycardia, Hypertrophic cardiomyopathy |
OMIM:618815 |
| Ethylene Glycol Poisoning |
|
Hypotension, Atrial fibrillation, Hypertension, Congestive heart failure, Tachycardia, Prolonged ... |
ORPHA:31826 |
| Ganglioneuroma |
|
Hypertension, Gastrointestinal hemorrhage |
ORPHA:251992 |
| Polyarteritis Nodosa |
|
Raynaud phenomenon, Hypertension, Pericarditis, Cardiomyopathy |
ORPHA:767 |
| Familial Hyperaldosteronism Type Ii |
|
Intracranial hemorrhage, Epistaxis, Hypertension |
ORPHA:404 |
| Nipah Virus Disease |
|
Hypotension |
ORPHA:99825 |
| Lipodystrophy, Familial Partial, Type 1 |
|
Hypertension |
OMIM:608600 |
| Non-Functioning Paraganglioma |
|
Palpitations, Hypertension associated with pheochromocytoma, Positive regitine blocking test, Sin... |
ORPHA:94080 |
| Tularemia |
|
Tachycardia |
ORPHA:3392 |
| Cocaine Intoxication |
|
Ventricular arrhythmia, Ischemic stroke, Prolonged QRS complex, Supraventricular arrhythmia, Hypo... |
ORPHA:90068 |
| Adrenocortical Carcinoma With Pure Aldosterone Hypersecretion |
|
Palpitations, Intracranial hemorrhage, Epistaxis, Hypertension, Abnormal T-wave |
ORPHA:231625 |
| Hereditary Coproporphyria |
|
Tachycardia |
ORPHA:79273 |
| Familial Cerebral Saccular Aneurysm |
|
Intracranial hemorrhage, Subarachnoid hemorrhage, Transient ischemic attack, Hypertension |
ORPHA:231160 |
| Ebstein Anomaly |
|
Atrial standstill, Ventricular preexcitation, Atrial fibrillation, Sudden cardiac death, Right bu... |
OMIM:224700 |
| Liddle Syndrome 1 |
|
Hypertension |
OMIM:177200 |
| Diffuse Cutaneous Mastocytosis |
|
Hypotension, Gastrointestinal hemorrhage |
ORPHA:79456 |
| Carnitine-Acylcarnitine Translocase Deficiency |
|
Hypotension, Arrhythmia, Cardiomyopathy, Ventricular tachycardia |
ORPHA:159 |
| Wild Type Attr Amyloidosis |
|
Arrhythmia, Orthostatic hypotension due to autonomic dysfunction, Myocardial infarction, Congesti... |
ORPHA:330001 |
| Acquired Aneurysmal Subarachnoid Hemorrhage |
|
Ischemic stroke, ST segment depression, Hypertension, Myocardial infarction, Cerebral hemorrhage,... |
ORPHA:90065 |
| Tropical Endomyocardial Fibrosis |
|
Atrial flutter, P pulmonale, Tricuspid regurgitation, Abnormal T-wave, Cardiogenic shock, Reduced... |
ORPHA:75565 |
| Familial Pseudohyperkalemia |
|
Hypertension |
ORPHA:90044 |
| Fructose-1,6-Bisphosphatase Deficiency |
|
Tachycardia |
OMIM:229700 |
| Familial Hyperaldosteronism Type Iii |
|
Intracranial hemorrhage, Prolonged QT interval, Epistaxis, Hypertension |
ORPHA:251274 |
| Coenzyme Q10 Deficiency, Primary, 8 |
|
Hypertension |
OMIM:616733 |
| Familial Hyperaldosteronism Type I |
|
Intracranial hemorrhage, Epistaxis, Hypertension |
ORPHA:403 |
| Neuroendocrine Tumor Of The Colon |
|
Palpitations, Right ventricular failure, Hypotension, Tricuspid regurgitation, Melena, Facial tel... |
ORPHA:100080 |
| Pseudoxanthoma Elasticum |
|
Gastrointestinal hemorrhage, Intermittent claudication, Angina pectoris, Restrictive cardiomyopat... |
OMIM:264800 |
| Mitochondrial Complex Iv Deficiency, Nuclear Type 4 |
|
Congestive heart failure, Bradycardia |
OMIM:619048 |
| Neuropathy, Hereditary Sensory And Autonomic, Type Iii |
|
Hypertension, Tachycardia, Orthostatic hypotension |
OMIM:223900 |
| Atherosclerosis-Deafness-Diabetes-Epilepsy-Nephropathy Syndrome |
|
Hypertension |
ORPHA:1192 |
| Nestor-Guillermo Progeria Syndrome |
|
Pulmonary arterial hypertension, Sinus tachycardia, Right bundle branch block, Hypertension |
OMIM:614008 |
| Moyamoya Angiopathy-Short Stature-Facial Dysmorphism-Hypergonadotropic Hypogonadism Syndrome |
|
Dilated cardiomyopathy, Cerebral hemorrhage, Ischemic stroke, Hypertension |
ORPHA:280679 |
| Congenital Fibrinogen Deficiency |
|
Tachycardia, Internal hemorrhage |
ORPHA:335 |
| Pituitary Adenoma 1, Multiple Types |
|
Cardiomyopathy, Hypertension |
OMIM:102200 |
| Coach Syndrome 2 |
|
Hypertension |
OMIM:619111 |
| Congenitally Corrected Transposition Of The Great Arteries |
|
Premature atrial contractions, Cardiac conduction abnormality, Supraventricular tachycardia with ... |
ORPHA:216694 |
| Nephroblastoma |
|
Hypertension |
ORPHA:654 |
| Rhabdoid Tumor |
|
Hypertension, Internal hemorrhage |
ORPHA:69077 |
| Erythrocytosis, Familial, 2 |
|
Hypotension, Cerebral hemorrhage |
OMIM:263400 |
| Coenzyme Q10 Deficiency, Primary, 5 |
|
Bradycardia |
OMIM:614654 |
| Apparent Mineralocorticoid Excess |
|
Hypertension |
OMIM:218030 |
| Abdominal Obesity-Metabolic Syndrome 4 |
|
Myocardial infarction, Hypertension |
OMIM:618620 |
| Primary Unilateral Adrenal Hyperplasia |
|
Palpitations, Epistaxis, Hypertension |
ORPHA:231580 |
| Lipodystrophy, Congenital Generalized, Type 4 |
|
Tachycardia, Atrial fibrillation, Prolonged QT interval, Bradycardia |
OMIM:613327 |
| Adult Acute Respiratory Distress Syndrome |
|
Hypotension, Vasculitis, Shock |
ORPHA:70578 |
| Late-Onset Familial Hypoaldosteronism |
|
Hypotension, Orthostatic hypotension |
ORPHA:556037 |
| Renal Nutcracker Syndrome |
|
Tachycardia, Orthostatic hypotension, Syncope |
ORPHA:71273 |
| Cerebral Autosomal Dominant Arteriopathy-Subcortical Infarcts-Leukoencephalopathy |
|
Ischemic stroke, Intracranial hemorrhage, Hypertension, Cerebral hemorrhage, Cerebral ischemia, L... |
ORPHA:136 |
| Double Outlet Right Ventricle |
|
Pulmonic stenosis, Heart murmur, Tachycardia |
ORPHA:3426 |
| Xfe Progeroid Syndrome |
|
Hypertension |
OMIM:610965 |
| Scorpion Envenomation |
|
Cardiogenic shock, Arrhythmia, Bundle branch block, Cardiac conduction abnormality, T-wave invers... |
ORPHA:466677 |
| Cushing Syndrome Due To Macronodular Adrenal Hyperplasia |
|
Hypertension |
ORPHA:189427 |
| Extracranial Carotid Artery Aneurysm |
|
Arteritis, Subarachnoid hemorrhage, Hypertension, Cerebral ischemia, Vasculitis |
ORPHA:494424 |
| Familial Dysautonomia |
|
Hypertension, Tachycardia, Orthostatic hypotension |
ORPHA:1764 |
| Illum Syndrome |
|
Bradycardia |
OMIM:208155 |
| Neuroleptic Malignant Syndrome |
|
Arrhythmia, Hypotension, Hypertensive crisis, Hypertension, Pulmonary embolism, Tachycardia, Brad... |
ORPHA:94093 |
| Porphyria Variegata |
|
Tachycardia, Hypertension |
ORPHA:79473 |
| Infant Botulism |
|
Hypotension, Cardiac arrest, Hypertension |
ORPHA:178478 |
| Cryoglobulinemia, Familial Mixed |
|
Hypertension |
OMIM:123550 |
| Corticosterone Methyloxidase Type I Deficiency |
|
Hypotension |
OMIM:203400 |
| Paroxysmal Hemicrania |
|
Hypertension |
ORPHA:157835 |
| Neuroendocrine Tumor Of The Rectum |
|
Palpitations, Right ventricular failure, Hematochezia, Hypotension, Tricuspid regurgitation, Mele... |
ORPHA:100081 |
| Neuroendocrine Tumor Of Anal Canal |
|
Palpitations, Right ventricular failure, Hematochezia, Hypotension, Tricuspid regurgitation, Mele... |
ORPHA:100082 |
| Hyperinsulinism Due To Hnf4A Deficiency |
|
Tachycardia |
ORPHA:263455 |
| Inhalational Anthrax |
|
Hypotension, Internal hemorrhage |
ORPHA:247257 |
| Renal Tubular Dysgenesis |
|
Hypotension |
OMIM:267430 |
| Malignant Hyperthermia Of Anesthesia |
|
Supraventricular tachycardia, Ventricular extrasystoles, Ventricular tachycardia, High-output con... |
ORPHA:423 |
| Isolated Ectopia Lentis |
|
Hypertension |
ORPHA:1885 |
| Ochoa Syndrome |
|
Hypertension |
ORPHA:2704 |
| 3-Methylglutaconic Aciduria, Type Viii |
|
Bradycardia |
OMIM:617248 |
| Vater-Like Defects With Pulmonary Hypertension, Laryngeal Webs, And Growth Deficiency |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:608406 |
| Juvenile Paget Disease |
|
Hypertension |
ORPHA:2801 |
| Congenital Isolated Acth Deficiency |
|
Hypotension |
ORPHA:199296 |
| Cholera |
|
Hypotension, Tachycardia, Hypovolemic shock |
ORPHA:173 |
| Polycystic Kidney Disease 2 With Or Without Polycystic Liver Disease |
|
Hypertension |
OMIM:613095 |
| Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 25 |
|
Palpitations, Atrioventricular block, Sinus bradycardia, Syncope |
OMIM:616812 |
| Riboflavin Transporter Deficiency |
|
Hypertension |
ORPHA:97229 |
| Polycythemia Vera |
|
Gastrointestinal hemorrhage, Intermittent claudication, Angina pectoris, Budd-Chiari syndrome, Ep... |
ORPHA:729 |
| Early-Onset Familial Hypoaldosteronism |
|
Hypotension, Orthostatic hypotension |
ORPHA:556030 |
| Metabolic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration |
|
Ventricular tachycardia, Ventricular fibrillation, Cardiac arrest, Prolonged QTc interval, Torsad... |
OMIM:616878 |
| Systemic Capillary Leak Syndrome |
|
Hypotension, Arrhythmia, Pericarditis, Myocarditis |
ORPHA:188 |
| Agenesis Of The Corpus Callosum And Congenital Lymphedema |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:613623 |
| Sepsis In Premature Infants |
|
Hypotension, Tachycardia, Bradycardia |
ORPHA:90051 |
| C3 Glomerulopathy |
|
Hypertension |
ORPHA:329918 |
| Neurodevelopmental Disorder With Seizures And Speech And Walking Impairment |
|
Hypotension |
OMIM:618480 |
| Fanconi Renotubular Syndrome 5 |
|
Hypertension |
OMIM:618913 |
| Bacterial Toxic-Shock Syndrome |
|
Hypotension, Tachycardia, Shock, Myocarditis, Capillary leak |
ORPHA:36234 |
| Pseudohypoaldosteronism, Type I, Autosomal Recessive |
|
Hypotension |
OMIM:264350 |
| Stiff Skin Syndrome |
|
Hypertension |
ORPHA:2833 |
| Fabry Disease |
|
Arrhythmia, Angina pectoris, Hypertension, Myocardial infarction, Congestive heart failure, Trans... |
OMIM:301500 |
| Systemic Mastocytosis With Associated Hematologic Neoplasm |
|
Hypotension, Tachycardia, Syncope |
ORPHA:98849 |
| Hemorrhagic Fever-Renal Syndrome |
|
Arrhythmia, Gastrointestinal hemorrhage, Intracranial hemorrhage, Subconjunctival hemorrhage, Hyp... |
ORPHA:340 |
| 16P12.1P12.3 Triplication Syndrome |
|
Tachycardia |
ORPHA:485405 |
| Dengue Fever |
|
Hypotension, Cerebral hemorrhage, Epistaxis, Gastrointestinal hemorrhage |
ORPHA:99828 |
| Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal |
|
Bradycardia |
OMIM:614498 |
| Ectopic Aldosterone-Producing Tumor |
|
Epistaxis, Hypertension |
ORPHA:231632 |
| Bronchial Neuroendocrine Tumor |
|
Cardiogenic shock, Palpitations, Right ventricular failure, Hypotension, Tricuspid regurgitation,... |
ORPHA:97287 |
| Primary Pigmented Nodular Adrenocortical Disease |
|
Hypertension |
ORPHA:189439 |
| Idiopathic Congenital Hypothyroidism |
|
Bradycardia |
ORPHA:95717 |
| Gitelman Syndrome |
|
Hypotension, Palpitations, Prolonged QT interval, Ventricular tachycardia |
OMIM:263800 |
| Hyperaldosteronism, Familial, Type Iii |
|
Hypertension |
OMIM:613677 |
| Pituitary Deficiency Due To Empty Sella Turcica Syndrome |
|
Hypotension |
ORPHA:91354 |
| Pseudohypoaldosteronism, Type I, Autosomal Dominant |
|
Hypotension |
OMIM:177735 |
| Acth-Independent Macronodular Adrenal Hyperplasia 2 |
|
Hypertension |
OMIM:615954 |
| Multiple Endocrine Neoplasia, Type Iia |
|
Palpitations, Hypertension |
OMIM:171400 |
| Primary Hyperaldosteronism-Seizures-Neurological Abnormalities Syndrome |
|
Intracranial hemorrhage, Epistaxis, Hypertension, Second degree atrioventricular block, Pulmonary... |
ORPHA:369929 |
| Nephronophthisis 2 |
|
Pulmonary insufficiency, Hypertension |
OMIM:602088 |
| Ogden Syndrome |
|
Arrhythmia, Ventricular extrasystoles, Ventricular tachycardia, Supraventricular tachycardia, Tor... |
OMIM:300855 |
| Acquired Von Willebrand Syndrome |
|
Joint hemorrhage, Aortic regurgitation, Gastrointestinal hemorrhage, Intracranial hemorrhage, Hyp... |
ORPHA:99147 |
| Severe Neurodegenerative Syndrome With Lipodystrophy |
|
Hypertension |
ORPHA:363400 |
| Myh7-Related Late-Onset Scapuloperoneal Muscular Dystrophy |
|
Arrhythmia, Abnormal left ventricular function, Hypertension, Heart murmur, Left anterior fascicu... |
ORPHA:437572 |
| Alagille Syndrome 2 |
|
Pulmonic stenosis, Hypertension |
OMIM:610205 |
| Renal Hypodysplasia/Aplasia 1 |
|
Hypertension |
OMIM:191830 |
| Arteriosclerosis, Severe Juvenile |
|
Myocardial infarction, Hypertension |
OMIM:208060 |
| Acute Intermittent Porphyria |
|
Tachycardia, Hypertension |
ORPHA:79276 |
| Gaucher Disease, Type I |
|
Epistaxis, Hypertension, Aortic valve stenosis, Pulmonary arterial hypertension, Mitral regurgita... |
OMIM:230800 |
| Fructose-1,6-Bisphosphatase Deficiency |
|
Tachycardia |
ORPHA:348 |
| Primary Lipodystrophy |
|
Angina pectoris, Hypertension, Congestive heart failure, Cardiomyopathy |
ORPHA:90970 |
| Adenine Phosphoribosyltransferase Deficiency |
|
Atrial fibrillation, Hypertension |
ORPHA:976 |
| Pediatric-Onset Graves Disease |
|
Palpitations, Sinus tachycardia, Atrial fibrillation, Hypertension, Congestive heart failure |
ORPHA:525731 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 3 |
|
Hypertension |
OMIM:612923 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 2 |
|
Hypertension |
OMIM:612922 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 5 |
|
Hypertension |
OMIM:612925 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 4 |
|
Hypertension |
OMIM:612924 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 6 |
|
Hypertension |
OMIM:612926 |
| Porphyria |
|
Hypertension |
ORPHA:738 |
| Ileal Neuroendocrine Tumor |
|
Cardiogenic shock, Palpitations, Arrhythmia, Right ventricular failure, Hypotension, Pulmonic ste... |
ORPHA:100078 |
| Jejunal Neuroendocrine Tumor |
|
Cardiogenic shock, Palpitations, Arrhythmia, Right ventricular failure, Hypotension, Pulmonic ste... |
ORPHA:100077 |
| Timothy Syndrome |
|
Bradycardia, Prolonged QT interval |
OMIM:601005 |
| Post-Traumatic Pituitary Deficiency |
|
Hypotension |
ORPHA:95619 |
| Necrotizing Enterocolitis |
|
Hypotension, Bradycardia, Shock |
ORPHA:391673 |
| Sporadic Pheochromocytoma/Secreting Paraganglioma |
|
Palpitations, Hypertension associated with pheochromocytoma, Positive regitine blocking test, Sin... |
ORPHA:276621 |
| Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 3 |
|
Arrhythmia, Bradycardia, Cardiomyopathy |
OMIM:609286 |
| Mucopolysaccharidosis-Like Syndrome With Congenital Heart Defects And Hematopoietic Disorders |
|
Tricuspid regurgitation, Congestive heart failure, Tachycardia, Pulmonary arterial hypertension, ... |
ORPHA:505248 |
| Lipodystrophy, Familial Partial, Type 3 |
|
Hypertension |
OMIM:604367 |
| Pseudo-Torch Syndrome 3 |
|
Cerebral hemorrhage, Hypertension |
OMIM:618886 |
| Spondylometaphyseal Dysplasia, Megarbane-Dagher-Melki Type |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:613320 |
| Frasier Syndrome |
|
Hypertension |
ORPHA:347 |
| Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type |
|
Bradycardia, Paroxysmal supraventricular tachycardia |
OMIM:601375 |
| Yellow Fever |
|
Hypotension, Congestive heart failure, Gastrointestinal hemorrhage, Arrhythmia |
ORPHA:99829 |
| Joubert Syndrome 14 |
|
Hypertension |
OMIM:614424 |
| Monosomy 18P |
|
Hypertension |
ORPHA:1598 |
| Mastocytosis |
|
Hypotension, Arrhythmia, Gastrointestinal hemorrhage, Telangiectasia of the skin |
ORPHA:98292 |
| Eisenmenger Syndrome |
|
Ventricular arrhythmia, Palpitations, Right ventricular failure, Hepatojugular reflux, Supraventr... |
ORPHA:97214 |
| Primary Aldosteronism, Seizures, And Neurologic Abnormalities |
|
Pulmonary arterial hypertension, Hypertension |
OMIM:615474 |
| Alport Syndrome 2, Autosomal Recessive |
|
Hypertension |
OMIM:203780 |
| Pigmented Nodular Adrenocortical Disease, Primary, 4 |
|
Hypertension |
OMIM:615830 |
| Nephronophthisis 1 |
|
Hypertension |
OMIM:256100 |
| Sudden Infant Death With Dysgenesis Of The Testes Syndrome |
|
Bradycardia |
OMIM:608800 |
| Microcephaly, Cerebellar Hypoplasia, And Cardiac Conduction Defect Syndrome |
|
Atrioventricular block, Bradycardia |
OMIM:614407 |
| Familial Hypoaldosteronism |
|
Hypotension, Orthostatic hypotension, Hypovolemia |
ORPHA:427 |
| Graft Versus Host Disease |
|
Tachycardia |
ORPHA:39812 |
| Scrub Typhus |
|
Hypotension, Myocarditis |
ORPHA:83317 |
| Colchicine Poisoning |
|
Cardiogenic shock, Arrhythmia, Hypovolemia, Hypotension, Congestive heart failure, Myocarditis |
ORPHA:31824 |
| Eosinophilic Granulomatosis With Polyangiitis |
|
Recurrent intrapulmonary hemorrhage, Hypertension, Myocardial infarction, Congestive heart failur... |
ORPHA:183 |
| Neuroendocrine Tumor Of Stomach |
|
Cardiogenic shock, Palpitations, Right ventricular failure, Hematemesis, Hypotension, Tricuspid r... |
ORPHA:100075 |
| Mirizzi Syndrome |
|
Tachycardia |
ORPHA:521219 |
| Aa Amyloidosis |
|
Hypotension |
ORPHA:85445 |
| Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations |
|
Punctate vasculitis skin lesions, Gastrointestinal hemorrhage, Cardiomyopathy, Hypertension, Reti... |
ORPHA:247691 |
| Congenital Hypothyroidism |
|
Hypotension, Arrhythmia, Hypertension |
ORPHA:442 |
| Pigmented Nodular Adrenocortical Disease, Primary, 1 |
|
Hypertension |
OMIM:610489 |
| Pigmented Nodular Adrenocortical Disease, Primary, 2 |
|
Hypertension |
OMIM:610475 |
| Short Stature, Facial Dysmorphism, And Skeletal Anomalies With Or Without Cardiac Anomalies 1 |
|
Pulmonic stenosis, Paroxysmal supraventricular tachycardia |
OMIM:617877 |
| Meningococcal Meningitis |
|
Hypotension, Shock |
ORPHA:33475 |
| Pseudoxanthoma Elasticum |
|
Gastrointestinal hemorrhage, Angina pectoris, Restrictive cardiomyopathy, Hypertension, Telangiec... |
ORPHA:758 |
| Arteritis, Familial Granulomatous, With Juvenile Polyarthritis |
|
Granulomatous coronary arteritis, Hypertension |
OMIM:108050 |
| Legionnaires Disease |
|
Hypotension, Arrhythmia, Pericarditis, Myocarditis |
ORPHA:549 |
| Buschke-Ollendorff Syndrome |
|
Hypertension |
ORPHA:1306 |
| Pparg-Related Familial Partial Lipodystrophy |
|
Congestive heart failure, Hypertension, Hypertrophic cardiomyopathy |
ORPHA:79083 |
| Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Portal hypertension, Hypertension |
OMIM:263200 |
| Diffuse Cutaneous Systemic Sclerosis |
|
Pulmonary arterial hypertension, Congestive heart failure, Hypertensive crisis, Telangiectasia of... |
ORPHA:220393 |
| Arterial Tortuosity Syndrome |
|
Ischemic stroke, Aortic regurgitation, Hypertension, Aortic valve stenosis, Telangiectases of the... |
OMIM:208050 |
| Duodenal Neuroendocrine Tumor |
|
Cardiogenic shock, Palpitations, Arrhythmia, Right ventricular failure, Hematemesis, Hypotension,... |
ORPHA:100076 |
| Familial Bicuspid Aortic Valve |
|
Heart murmur, Hypertension, Aortic valve stenosis, Aortic regurgitation |
ORPHA:402075 |
| Pseudo-Torch Syndrome 2 |
|
Cerebral hemorrhage, Bradycardia |
OMIM:617397 |
| Acth-Independent Macronodular Adrenal Hyperplasia |
|
Hypertension |
OMIM:219080 |
| Schimke Immunoosseous Dysplasia |
|
Transient ischemic attack, Cerebral ischemia, Hypertension |
OMIM:242900 |
| Apparent Mineralocorticoid Excess |
|
Hypertension |
ORPHA:320 |
| Telangiectasia, Hereditary Hemorrhagic, Type 2 |
|
Conjunctival telangiectasia, Ischemic stroke, Nail bed telangiectasia, Lip telangiectasia, Hemate... |
OMIM:600376 |
| Primary Progressive Freezing Gait |
|
Hypertension |
ORPHA:75567 |
| Aorta Coarctation |
|
Pulmonary arterial hypertension, Congestive heart failure, Hypertension |
ORPHA:1457 |
| Popov-Chang syndrome |
|
Pulmonic stenosis, Hypertension |
OMIM:618428 |
| Tubulointerstitial Kidney Disease, Autosomal Dominant, 2 |
|
Hypotension, Hypertension |
OMIM:174000 |
| Glutamine Deficiency, Congenital |
|
Bradycardia |
OMIM:610015 |
| Cushing Disease |
|
Hypertension, Cardiomyopathy, Telangiectasia of the skin |
ORPHA:96253 |
| Bardet-Biedl Syndrome |
|
Hypertension |
ORPHA:110 |
| Whipple Disease |
|
Pericarditis, Gastrointestinal hemorrhage, Hypotension, Myocardial infarction, Myocarditis |
ORPHA:3452 |
| Aggressive Systemic Mastocytosis |
|
Hypotension, Portal hypertension, Gastrointestinal hemorrhage |
ORPHA:98850 |
| Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 2 |
|
Arrhythmia, Hypertension, Hypertrophic cardiomyopathy |
OMIM:614052 |
| Schimke Immuno-Osseous Dysplasia |
|
Ischemic stroke, Hypertension, Congestive heart failure, Cerebral ischemia, Pulmonary arterial hy... |
ORPHA:1830 |
| Congenital Hypothyroidism Due To Maternal Intake Of Antithyroid Drugs |
|
Bradycardia |
ORPHA:226313 |
| Nephronophthisis-Like Nephropathy 1 |
|
Hypertension |
OMIM:613159 |
| Hereditary Pheochromocytoma-Paraganglioma |
|
Palpitations, Hypertension associated with pheochromocytoma, Positive regitine blocking test, Sin... |
ORPHA:29072 |
| Congenital Enterovirus Infection |
|
Hypotension, Cardiomyopathy, Myocarditis |
ORPHA:292 |
| Neuroblastoma, Susceptibility To, 1 |
|
Hypertension |
OMIM:256700 |
| Methylcobalamin Deficiency Type Cble |
|
Hypertension |
ORPHA:2169 |
| Glossopharyngeal Neuralgia |
|
Bradycardia, Jaw claudication, Syncope |
ORPHA:221098 |
| Acquired Generalized Lipodystrophy |
|
Hypertension, Abnormal cardiovascular system physiology, Cardiomyopathy |
ORPHA:79086 |
| Adrenocortical Carcinoma |
|
Palpitations, Hypertension |
ORPHA:1501 |
| Familial Thyroid Dyshormonogenesis |
|
Bradycardia |
ORPHA:95716 |
| Staphylococcal Necrotizing Pneumonia |
|
Hypotension, Shock |
ORPHA:36238 |
| Tatton-Brown-Rahman Syndrome |
|
Supraventricular tachycardia with an accessory connection mediated pathway, Mitral regurgitation,... |
ORPHA:404443 |
| Autosomal Dominant Hypocalcemia |
|
Hypotension, Congestive heart failure, Arrhythmia |
ORPHA:428 |
| Hennekam-Beemer Syndrome |
|
Hypotension, Arrhythmia, Telangiectasia of the skin |
ORPHA:2135 |
| Beta-Ketothiolase Deficiency |
|
Hypotension, Hypertension |
ORPHA:134 |
| Poliomyelitis |
|
Hypotension, Hypertension, Hypovolemic shock |
ORPHA:2912 |
| Coach Syndrome 1 |
|
Portal hypertension, Hypertension |
OMIM:216360 |
| Pde4D Haploinsufficiency Syndrome |
|
Hypotension |
ORPHA:439822 |
| Renal Hypoplasia |
|
Hypertension |
ORPHA:93101 |
| Fabry Disease |
|
Conjunctival telangiectasia, Arrhythmia, Bundle branch block, Angina pectoris, Mitral regurgitati... |
ORPHA:324 |
| Acitretin/Etretinate Embryopathy |
|
