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CDC/NIH Web Information Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

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Heart, Lung, Blood and Sleep Disorders

Last data update: Apr 15, 2024. (Total: 8777 Documents)
   dataset      
Records 1-27 (of 27 Records)
CDC/NIH Web Information
Modeling Hypertrophic Cardiomyopathy in a Dish
NIH Director's Blog, November 8, 2018 Brand
Angina
From NHLBI health topic site Brand
Cardiomyopathy
From NHLBI health topic site Brand
Diabetic Heart Disease
From NHLBI health topic site Brand
Heart Disease in Women
From NHLBI health topic site Brand
Heart Palpitations
From NHLBI health topic site Brand
Peripartum cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Dilated cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy cataract hip spine disease
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy diabetes deafness
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy dilated with conduction defect type 1
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy due to anthracyclines
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy and deafness due to tRNA lysine gene mutation
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy hypogonadism metabolic anomalies
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy spherocytosis
From NCATS Genetic and Rare Diseases Information Center Brand
Hypogonadism cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Familial dilated cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Dilated cardiomyopathy with hypergonadotropic hypogonadism
From NCATS Genetic and Rare Diseases Information Center Brand
Microcephaly-cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Spine rigid cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy dilated with woolly hair and keratoderma
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy dilated with conduction defect type 2
From NCATS Genetic and Rare Diseases Information Center Brand
Doxorubicin induced cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Familial hypertrophic cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy, fatal fetal, due to myocardial calcification
From NCATS Genetic and Rare Diseases Information Center Brand
Infantile histiocytoid cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules
From NCATS Genetic and Rare Diseases Information Center Brand
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