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21ohd chf classes classification congestive diagnosis endocrinology genetics nyha pathophysiology pediatrics stages staging
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency ... endocrinology #peds
In order to better classify heart failure, the American College of Cardiology Foundation and the American
American College of Cardiology ... or signs of heart ... #Diagnosis #Cardiology ... CHF #Congestive #HeartFailure ... Classes #NYHA #ACCAHA
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