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Nume Cosyntropin

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Boli A-Z Acth Deficiency, Isolated Adrenal Carcinoma Adrenal Cortex Disease Adrenal Cortical Hypofunction Adrenal Gland Disease Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Alcohol Abuse Alcohol Dependence Arteries, Anomalies of Arteriosclerosis Asthma Ataxia Neuropathy Spectrum Atrophic Muscular Disease Autoimmune Addison Disease Autoimmune Disease Autonomic Dysfunction Autonomic Nervous System Disease Autosomal Dominant Polycystic Kidney Disease Brain Injury Cardiomyopathy, Dilated, 3b Central Nervous System Disease Chromosomal Disease Coronary Artery Anomaly Coronary Heart Disease 1 Dysautonomia Encephalopathy Epilepsy Familial Lcat Deficiency Genitourinary Tract Anomalies Glomerulonephritis Gonadal Disease Headache Head Injury Heart Disease Heart Valve Disease Hyperandrogenism Hypoadrenalism Hypoadrenocorticism, Familial Hypoaldosteronism Hypoglycemia Hypolipoproteinemia Hypopituitarism Hypothalamic Disease Hypotonia Immune System Disease Infantile Epileptic Encephalopathy Intracranial Hypertension Ischemia Ischemic Heart Disease Kidney Disease Lecithin:cholesterol Acyltransferase Deficiency Lipid Metabolism Disorder Lipoid Congenital Adrenal Hyperplasia Liver Cirrhosis Liver Disease Membranous Nephropathy Meningitis Mitral Valve Insufficiency Muscle Disorders Muscle Tissue Disease Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy, Duchenne Type Myopathy Myotonia Congenita, Autosomal Recessive Nervous System Disease Neurofibromatosis, Type Ii Neuromuscular Disease Oculocerebral Syndrome with Hypopigmentation Orthostatic Intolerance Ovarian Cyst Ovarian Disease Overnutrition Pain Agnosia Pituitary Gland Disease Polycystic Kidney Disease Polycystic Ovary Syndrome Polycystic Ovary Syndrome 1 Postural Orthostatic Tachycardia Syndrome Prader-Willi Syndrome Secondary Adrenal Insufficiency Seizure Disorder Sex Differentiation Disease Substance Abuse Trichohepatoenteric Syndrome 1 Urinary System Disease West Syndrome
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