Browse Medical Conditions by Category: Nutritional and Metabolic Diseases
- Abetalipoproteinemia
- Achlorhydria
- Acid-Base Imbalance
- Acidosis
- Acidosis, Lactic
- Acidosis, Renal Tubular
- Acidosis, Respiratory
- Adiposis Dolorosa
- Adrenal Hyperplasia, Congenital
- Adrenoleukodystrophy
- Albinism
- Albinism, Ocular
- Albinism, Oculocutaneous
- Alexander Disease
- Alkalosis
- Alkalosis, Respiratory
- Alkaptonuria
- alpha-Mannosidosis
- Amino Acid Metabolism, Inborn Errors
- Amyloid Neuropathies
- Amyloid Neuropathies, Familial
- Amyloidosis
- Amyloidosis, Familial
- Amyotrophic Lateral Sclerosis
- Anemia, Iron-Deficiency
- Anemia, Pernicious
- Argininosuccinic Aciduria
- Arthritis, Gouty
- Ascorbic Acid Deficiency
- Aspartylglucosaminuria
- Ataxia Telangiectasia
- Avitaminosis
- Barth Syndrome
- Beriberi
- beta-Mannosidosis
- Biotinidase Deficiency
- Blind Loop Syndrome
- Bloom Syndrome
- Bone Demineralization, Pathologic
- Bone Diseases, Metabolic
- Brain Diseases, Metabolic
- Brain Diseases, Metabolic, Inborn
- Calcinosis
- Calciphylaxis
- Calcium Metabolism Disorders
- Canavan Disease
- Carbamoyl-Phosphate Synthase I Deficiency Disease
- Carbohydrate Metabolism, Inborn Errors
- Celiac Disease
- Cerebral Amyloid Angiopathy
- Cerebral Amyloid Angiopathy, Familial
- Child Nutrition Disorders
- Cholesterol Ester Storage Disease
- Choline Deficiency
- Chondrodysplasia Punctata, Rhizomelic
- Chronic Kidney Disease-Mineral and Bone Disorder
- Citrullinemia
- Cockayne Syndrome
- Collagenous Sprue
- Colorectal Neoplasms, Hereditary Nonpolyposis
- Congenital Disorders of Glycosylation
- Congenital Hyperinsulinism
- Coproporphyria, Hereditary
- CREST Syndrome
- Crigler-Najjar Syndrome
- Cystinosis
- Deficiency Diseases
- Dehydration
- Diabetes, Gestational
- Diabetes Mellitus
- Diabetes Mellitus, Experimental
- Diabetes Mellitus, Lipoatrophic
- Diabetes Mellitus, Type 1
- Diabetes Mellitus, Type 2
- Diabetic Ketoacidosis
- DNA Repair-Deficiency Disorders
- Dyslipidemias
- Fabry Disease
- Familial Hypophosphatemic Rickets
- Familial Multiple Lipomatosis
- Fanconi Anemia
- Farber Lipogranulomatosis
- Fetal Nutrition Disorders
- Folic Acid Deficiency
- Friedreich Ataxia
- Frontotemporal Dementia
- Frontotemporal Lobar Degeneration
- Fructose Intolerance
- Fructose Metabolism, Inborn Errors
- Fucosidosis
- Galactosemias
- Gangliosidoses
- Gangliosidoses, GM2
- Gangliosidosis, GM1
- Gaucher Disease
- Gilbert Disease
- Glucose Intolerance
- Glucose Metabolism Disorders
- Glucosephosphate Dehydrogenase Deficiency
- Glycogen Storage Disease
- Glycogen Storage Disease Type I
- Glycogen Storage Disease Type II
- Glycogen Storage Disease Type IIb
- Glycogen Storage Disease Type III
- Glycogen Storage Disease Type IV
- Glycogen Storage Disease Type V
- Glycogen Storage Disease Type VI
- Glycogen Storage Disease Type VII
- Glycogen Storage Disease Type VIII
- Glycosuria, Renal
- Gout
- Hemochromatosis
- Hemosiderosis
- Hepatic Encephalopathy
- Hepatolenticular Degeneration
- Hereditary Central Nervous System Demyelinating Diseases
- Hermanski-Pudlak Syndrome
- HIV-Associated Lipodystrophy Syndrome
- HIV Wasting Syndrome
- Homocystinuria
- Hyperargininemia
- Hypercalcemia
- Hypercholesterolemia
- Hyperferritinemia
- Hyperglycemia
- Hyperhomocysteinemia
- Hyperinsulinism
- Hyperkalemia
- Hyperlactatemia
- Hyperlipidemia, Familial Combined
- Hyperlipidemias
- Hyperlipoproteinemias
- Hyperlipoproteinemia Type I
- Hyperlipoproteinemia Type II
- Hyperlipoproteinemia Type III
- Hyperlipoproteinemia Type IV
- Hyperlipoproteinemia Type V
- Hypernatremia
- Hyperoxaluria, Primary
- Hyperphosphatemia
- Hypertriglyceridemia
- Hypertriglyceridemic Waist
- Hypervitaminosis A
- Hypoalphalipoproteinemias
- Hypobetalipoproteinemia, Familial, Apolipoprotein B
- Hypobetalipoproteinemias
- Hypocalcemia
- Hypoglycemia
- Hypokalemia
- Hypokalemic Periodic Paralysis
- Hypolipoproteinemias
- Hyponatremia
- Hypophosphatasia
- Hypophosphatemia
- Hypophosphatemia, Familial
- Ichthyosis, X-Linked
- Immunoglobulin Light-chain Amyloidosis
- Inappropriate ADH Syndrome
- Infant Nutrition Disorders
- Insulin Resistance
- Iron Metabolism Disorders
- Iron Overload
- Kearns-Sayre Syndrome
- Kernicterus
- Ketosis
- Kwashiorkor
- Lactose Intolerance
- Latent Autoimmune Diabetes in Adults
- Lecithin Cholesterol Acyltransferase Deficiency
- Leigh Disease
- Lesch-Nyhan Syndrome
- Leukodystrophy, Globoid Cell
- Leukodystrophy, Metachromatic
- Li-Fraumeni Syndrome
- Lipid Metabolism Disorders
- Lipid Metabolism, Inborn Errors
- Lipidoses
- Lipodystrophy
- Lipodystrophy, Congenital Generalized
- Lipodystrophy, Familial Partial
- Lipomatosis
- Lipomatosis, Multiple Symmetrical
- Lysosomal Storage Diseases
- Magnesium Deficiency
- Malabsorption Syndromes
- Malnutrition
- Mannosidase Deficiency Diseases
- Maple Syrup Urine Disease
- MELAS Syndrome
- Menkes Kinky Hair Syndrome
- Metabolic Diseases
- Metabolic Syndrome
- Metabolism, Inborn Errors
- Metal Metabolism, Inborn Errors
- Mevalonate Kinase Deficiency
- Mineralocorticoid Excess Syndrome, Apparent
- Mitochondrial Diseases
- Mitochondrial Encephalomyopathies
- Mitochondrial Myopathies
- Monckeberg Medial Calcific Sclerosis