• Abetalipoproteinemia   2 studies
• Achlorhydria   4 studies
• Acidosis   25 studies
• Acidosis, Lactic   14 studies
• Acidosis, Respiratory   1 study
• Adrenal Hyperplasia, Congenital   16 studies
• Adrenoleukodystrophy   15 studies
• Albinism   6 studies
• Albinism, Ocular   1 study
• Albinism, Oculocutaneous   5 studies
• Alkalosis   3 studies
• Alkaptonuria   2 studies
• Alpha-Mannosidosis   5 studies
• Amino Acid Metabolism, Inborn Errors   47 studies
• Amyloid Neuropathies   2 studies
• Amyloid Neuropathies, Familial   2 studies
• Amyloidosis   96 studies
• Amyloidosis, Familial   2 studies
• Anemia, Iron-Deficiency   43 studies
• Arthritis, Gouty   4 studies
• Ataxia Telangiectasia   32 studies
• Avitaminosis   86 studies
• Bloom Syndrome   1 study
• Brain Diseases, Metabolic   192 studies
• Brain Diseases, Metabolic, Inborn   173 studies
• Calcinosis   5 studies
• Carbamoyl-Phosphate Synthase I Deficiency Disease   1 study
• Celiac Disease   25 studies
• Cerebral Amyloid Angiopathy   1 study
• Cholesterol Ester Storage Disease   3 studies
• Citrullinemia   2 studies
• Cockayne Syndrome   1 study
• Colorectal Neoplasms, Hereditary Nonpolyposis   17 studies
• Crigler-Najjar Syndrome   1 study
• Cystinosis   9 studies
• Cystinuria   2 studies
• Deficiency Diseases   142 studies
• Dehydration   15 studies
• Diabetes Mellitus   2976 studies
• Diabetes Mellitus, Experimental   1 study
• Diabetes Mellitus, Type 1   414 studies
• Diabetes Mellitus, Type 2   1534 studies
• Diabetes, Gestational   32 studies
• Diabetic Ketoacidosis   6 studies
• Dihydropyrimidine Dehydrogenase Deficiency   5 studies
• Dyslipidemias   717 studies
• Fabry Disease   42 studies
• Fanconi Anemia   31 studies
• Fanconi Syndrome   7 studies
• Folic Acid Deficiency   1 study
• Friedreich Ataxia   9 studies
• Fucosidosis   4 studies
• Galactosemias   2 studies
• Gangliosidoses   8 studies
• Gangliosidoses, GM2   7 studies
• Gangliosidosis, GM1   3 studies
• Gaucher Disease   32 studies
• Glucose Intolerance   91 studies
• Glucose Metabolism Disorders   2665 studies
• Glucosephosphate Dehydrogenase Deficiency   2 studies
• Glycogen Storage Disease   32 studies
• Glycogen Storage Disease Type I   8 studies
• Glycogen Storage Disease Type II   30 studies
• Glycogen Storage Disease Type VII   1 study
• Gout   22 studies
• Hemochromatosis   22 studies
• Hemosiderosis   13 studies
• Hepatic Encephalopathy   21 studies
• Hepatolenticular Degeneration   4 studies
• Hermanski-Pudlak Syndrome   4 studies
• HIV Wasting Syndrome   15 studies
• HIV-Associated Lipodystrophy Syndrome   19 studies
• Homocystinuria   2 studies
• Hypercalcemia   19 studies
• Hypercholesterolemia   363 studies
• Hyperglycemia   229 studies
• Hyperhomocysteinemia   12 studies
• Hyperinsulinism   348 studies
• Hyperkalemia   5 studies
• Hyperlipidemia, Familial Combined   21 studies
• Hyperlipidemias   550 studies
• Hyperlipoproteinemia Type II   40 studies
• Hyperlipoproteinemia Type III   3 studies
• Hyperlipoproteinemia Type IV   4 studies
• Hyperlipoproteinemia Type V   3 studies
• Hyperlipoproteinemias   51 studies
• Hypernatremia   4 studies
• Hyperoxaluria, Primary   6 studies
• Hyperphosphatemia   34 studies
• Hypertriglyceridemia   62 studies
• Hypoalphalipoproteinemias   4 studies
• Hypobetalipoproteinemias   4 studies
• Hypocalcemia   15 studies
• Hypoglycemia   114 studies
• Hypokalemia   5 studies
• Hypokalemic Periodic Paralysis   2 studies
• Hypolipoproteinemias   8 studies
• Hyponatremia   29 studies
• Hypophosphatasia   2 studies
• Hypophosphatemia   8 studies
• Hypophosphatemia, Familial   4 studies
• Hypophosphatemic Rickets, X-Linked Dominant   3 studies
• Ichthyosis, X-Linked   1 study
• Inappropriate ADH Syndrome   7 studies
• Insulin Resistance   461 studies
• Iron Metabolism Disorders   101 studies
• Iron Overload   65 studies
• Ketosis   6 studies
• Kwashiorkor   2 studies
• Lactose Intolerance   3 studies
• Lesch-Nyhan Syndrome   1 study
• Leukodystrophy, Globoid Cell   6 studies
• Leukodystrophy, Metachromatic   10 studies
• Li-Fraumeni Syndrome   1 study
• Lipid Metabolism Disorders   830 studies
• Lipid Metabolism, Inborn Errors   177 studies
• Lipidoses   96 studies
• Lipodystrophy   73 studies
• Lysosomal Storage Diseases   159 studies
• Malabsorption Syndromes   45 studies
• Malnutrition   255 studies
• Mannosidase Deficiency Diseases   5 studies
• MELAS Syndrome   2 studies
• Menkes Kinky Hair Syndrome   1 study
• Metabolic Diseases   4031 studies
• Metabolic Syndrome X   95 studies
• Metabolism, Inborn Errors   437 studies
• Mevalonate Kinase Deficiency   1 study
• Mineralocorticoid Excess Syndrome, Apparent   1 study
• Mitochondrial Diseases   19 studies
• Mitochondrial Myopathies   4 studies
• Mucolipidoses   4 studies
• Mucopolysaccharidoses   29 studies
• Mucopolysaccharidosis I   19 studies
• Mucopolysaccharidosis II   6 studies
• Mucopolysaccharidosis IV   1 study
• Mucopolysaccharidosis VI   9 studies
• Mucopolysaccharidosis VII   1 study
• Nephrocalcinosis   2 studies
• Neuronal Ceroid-Lipofuscinoses   5 studies
• Niemann-Pick Disease, Type A   8 studies
• Niemann-Pick Disease, Type B   1 study
• Niemann-Pick Disease, Type C   8 studies
• Niemann-Pick Diseases   8 studies
• Nutrition Disorders   1238 studies
• Obesity   1240 studies
• Obesity Hypoventilation Syndrome   2 studies
• Obesity, Morbid   65 studies
• Oculocerebrorenal Syndrome   2 studies
• Optic Atrophy, Hereditary, Leber   2 studies
• Ornithine Carbamoyltransferase Deficiency Disease   5 studies
• Osteomalacia   5 studies
• Overnutrition   1018 studies
• Paralysis, Hyperkalemic Periodic   1 study
• Peroxisomal Disorders   16 studies
• Persistent Hyperinsulinemia Hypoglycemia of Infancy   2 studies
• Phenylketonuria, Maternal   1 study
• Phenylketonurias   18 studies
• Porphyria Cutanea Tarda   3 studies
• Porphyria, Acute Intermittent   3 studies
• Porphyria, Erythropoietic   15 studies
• Porphyrias   15 studies
• Porphyrias, Hepatic   8 studies
• Prader-Willi Syndrome   12 studies
• Prediabetic State   52 studies
• Progeria   3 studies
• Protein Deficiency   5 studies
• Protein-Energy Malnutrition   5 studies
• Protoporphyria, Erythropoietic   3 studies
• Pseudohypoaldosteronism   4 studies
• Pseudohypoparathyroidism   4 studies
• Pseudopseudohypoparathyroidism   2 studies
• Purine-Pyrimidine Metabolism, Inborn Errors   21 studies
• Refsum Disease   2 studies
• Refsum Disease, Infantile   2 studies
• Renal Osteodystrophy   13 studies
• Rickets   23 studies
• Sandhoff Disease   6 studies
• Severe Combined Immunodeficiency   21 studies
• Smith-Lemli-Opitz Syndrome   9 studies
• Sphingolipidoses   93 studies
• Starvation   4 studies
• Steatorrhea   10 studies
• Tangier Disease   1 study
• Tay-Sachs Disease   7 studies
• Tyrosinemias   2 studies
• Vitamin A Deficiency   12 studies
• Vitamin B 12 Deficiency   9 studies
• Vitamin D Deficiency   72 studies
• Wasting Syndrome   15 studies
• Water Intoxication   2 studies
• Water-Electrolyte Imbalance   71 studies
• Werner Syndrome   1 study
• Wolman Disease   3 studies
• Xanthomatosis   2 studies
• Xanthomatosis, Cerebrotendinous   2 studies
• Xeroderma Pigmentosum   6 studies
• Zellweger Syndrome   2 studies
  

Clinical Trials Authorship and Review

Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.