February is Heart Month

CDC/NIH Web Information Database|Home|PHGKB

Recent data suggest that more than 1.3 million people (1 in 250) in the United States have FH and that many of them are undertreated, even when they know they have high cholesterol.

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CDC/NIH Web Information
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome From NCATS Genetic and Rare Diseases Information Center
Chronic thromboembolic pulmonary hypertension From NCATS Genetic and Rare Diseases Information Center
ANCA-associated vasculitis From NCATS Genetic and Rare Diseases Information Center
Primary orthostatic hypotension From NCATS Genetic and Rare Diseases Information Center
Pediatric hypertension From NCATS Genetic and Rare Diseases Information Center
Bow hunter's stroke From NCATS Genetic and Rare Diseases Information Center
Hereditary endotheliopathy, retinopathy, nephropathy, and stroke From NCATS Genetic and Rare Diseases Information Center
Familial pulmonary arterial hypertension leucopenia and atrial septal defect From NCATS Genetic and Rare Diseases Information Center
Neonatal stroke From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 11 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 10 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 9 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 6 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 5 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 4 From NCATS Genetic and Rare Diseases Information Center
Familial arteriosclerotic leukoencephalopathy, alopecia, lumbago without arterial hypertension From NCATS Genetic and Rare Diseases Information Center
Tetralogy of fallot and glaucoma From NCATS Genetic and Rare Diseases Information Center
Aneurysm, intracranial berry, 2 From NCATS Genetic and Rare Diseases Information Center
Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules From NCATS Genetic and Rare Diseases Information Center
Aortic aneurysm, familial thoracic 4 From NCATS Genetic and Rare Diseases Information Center
Familial atrial fibrillation From NCATS Genetic and Rare Diseases Information Center
Anterior spinal artery stroke From NCATS Genetic and Rare Diseases Information Center
Infantile histiocytoid cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Sudden Arrhythmia Death Syndrome From NCATS Genetic and Rare Diseases Information Center
Abdominal obesity metabolic syndrome From NCATS Genetic and Rare Diseases Information Center
Abdominal aortic aneurysm From NCATS Genetic and Rare Diseases Information Center
Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy, fatal fetal, due to myocardial calcification From NCATS Genetic and Rare Diseases Information Center
Hypersensitivity vasculitis From NCATS Genetic and Rare Diseases Information Center
Rheumatoid vasculitis From NCATS Genetic and Rare Diseases Information Center
Renoprival hypertension From NCATS Genetic and Rare Diseases Information Center
Pulmonary arterial hypertension From NCATS Genetic and Rare Diseases Information Center
Prinzmetal's variant angina From NCATS Genetic and Rare Diseases Information Center
Patent ductus arteriosus From NCATS Genetic and Rare Diseases Information Center
Familial hypertrophic cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Neurogenic hypertension From NCATS Genetic and Rare Diseases Information Center
Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes From NCATS Genetic and Rare Diseases Information Center
Marfan syndrome From NCATS Genetic and Rare Diseases Information Center
Lymphocytic vasculitis From NCATS Genetic and Rare Diseases Information Center
Kawasaki disease From NCATS Genetic and Rare Diseases Information Center
Kallikrein hypertension From NCATS Genetic and Rare Diseases Information Center
Hypocomplementemic urticarial vasculitis From NCATS Genetic and Rare Diseases Information Center
Infective endocarditis From NCATS Genetic and Rare Diseases Information Center
Doxorubicin induced cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Coronary artery aneurysm From NCATS Genetic and Rare Diseases Information Center
Congenital heart block From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy dilated with conduction defect type 2 From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy dilated with woolly hair and keratoderma From NCATS Genetic and Rare Diseases Information Center
Vein of Galen aneurysm From NCATS Genetic and Rare Diseases Information Center
Spine rigid cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Spastic angina with healthy coronary artery From NCATS Genetic and Rare Diseases Information Center
Progressive familial heart block type 2 From NCATS Genetic and Rare Diseases Information Center
Shoulder and thorax deformity congenital heart disease From NCATS Genetic and Rare Diseases Information Center
Short stature valvular heart disease From NCATS Genetic and Rare Diseases Information Center
Short limbs abnormal face congenital heart disease From NCATS Genetic and Rare Diseases Information Center
Portal hypertension due to infrahepatic block From NCATS Genetic and Rare Diseases Information Center
Phocomelia ectrodactyly deafness sinus arrhythmia From NCATS Genetic and Rare Diseases Information Center
Mitral valve prolapse, familial, X-linked From NCATS Genetic and Rare Diseases Information Center
Mitral valve prolapse, familial, autosomal dominant From NCATS Genetic and Rare Diseases Information Center
Microcephaly-cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Dilated cardiomyopathy with hypergonadotropic hypogonadism From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 3 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 2 From NCATS Genetic and Rare Diseases Information Center
Long QT syndrome 1 From NCATS Genetic and Rare Diseases Information Center
Familial dilated cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Hypogonadism cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Hypertelorism and tetralogy of Fallot From NCATS Genetic and Rare Diseases Information Center
Hirschsprung disease polydactyly heart disease From NCATS Genetic and Rare Diseases Information Center
Progressive familial heart block type 1B From NCATS Genetic and Rare Diseases Information Center
Fetal left ventricular aneurysm From NCATS Genetic and Rare Diseases Information Center
Familial thoracic aortic aneurysm and dissection From NCATS Genetic and Rare Diseases Information Center
Tetralogy of Fallot From NCATS Genetic and Rare Diseases Information Center
Duodenal atresia tetralogy of Fallot From NCATS Genetic and Rare Diseases Information Center
Congenital heart disease radio ulnar synostosis mental retardation From NCATS Genetic and Rare Diseases Information Center
Congenital heart disease ptosis hypodontia craniostosis From NCATS Genetic and Rare Diseases Information Center
Cleft palate heart disease polydactyly absent tibia From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy spherocytosis From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy hypogonadism metabolic anomalies From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy and deafness due to tRNA lysine gene mutation From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy due to anthracyclines From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy dilated with conduction defect type 1 From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy diabetes deafness From NCATS Genetic and Rare Diseases Information Center
Cardiomyopathy cataract hip spine disease From NCATS Genetic and Rare Diseases Information Center
Progressive familial heart block type 1A From NCATS Genetic and Rare Diseases Information Center
Brachydactyly with hypertension From NCATS Genetic and Rare Diseases Information Center
Aneurysm of sinus of Valsalva From NCATS Genetic and Rare Diseases Information Center
Camptodactyly arthropathy coxa vara pericarditis syndrome From NCATS Genetic and Rare Diseases Information Center
Dilated cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Peripartum cardiomyopathy From NCATS Genetic and Rare Diseases Information Center
Modeling Hypertrophic Cardiomyopathy in a Dish NIH Director's Blog, November 8, 2018
Gene mutation points to new way to fight diabetes, obesity, heart disease NIH, October 9, 2018
Sleep Studies  From NHLBI health topic site
Obesity Hypoventilation Syndrome From NHLBI health topic site
Thoracentesis  From NHLBI health topic site
Pulmonary Hypertension  From NHLBI health topic site
Pulmonary Embolism  From NHLBI health topic site
Pneumonia  From NHLBI health topic site
Lung Transplant  From NHLBI health topic site
Idiopathic Pulmonary Fibrosis From NHLBI health topic site
Pleurisy and Other Pleural Disorders From NHLBI health topic site