Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (4)
- Achlorhydria (6)
- Acid-Base Imbalance (290)
- Acidosis (311)
- Acidosis, Lactic (52)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (18)
- Adiposis Dolorosa (6)
- Adrenal Hyperplasia, Congenital (143)
- Adrenoleukodystrophy (64)
- Albinism (38)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (4)
- Alkalosis (25)
- Alkalosis, Respiratory (8)
- Alkaptonuria (9)
- Amino Acid Metabolism, Inborn Errors (335)
- Amyloid Neuropathies (51)
- Amyloid Neuropathies, Familial (45)
- Amyloidosis (828)
- Amyloidosis, Familial (77)
- Amyotrophic Lateral Sclerosis (957)
- Anemia, Iron-Deficiency (743)
- Anemia, Pernicious (5)
- Argininosuccinic Aciduria (9)
- Arthritis, Gouty (42)
- Ascorbic Acid Deficiency (16)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (46)
- Avitaminosis (1,035)
- Barth Syndrome (8)
- Beriberi (27)
- Biotinidase Deficiency (5)
- Blind Loop Syndrome (33)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,800)
- Brain Diseases, Metabolic (1,206)
- Brain Diseases, Metabolic, Inborn (1,010)
- CREST Syndrome (9)
- Calcinosis (360)
- Calciphylaxis (16)
- Calcium Metabolism Disorders (575)
- Canavan Disease (10)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (9)
- Carbohydrate Metabolism, Inborn Errors (601)
- Celiac Disease (326)
- Cerebral Amyloid Angiopathy (27)
- Cerebral Amyloid Angiopathy, Familial (27)
- Child Nutrition Disorders (116)
- Cholesterol Ester Storage Disease (33)
- Choline Deficiency (5)
- Chondrodysplasia Punctata, Rhizomelic (3)
- Chronic Kidney Disease-Mineral and Bone Disorder (53)
- Citrullinemia (12)
- Cockayne Syndrome (10)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (93)
- Congenital Disorders of Glycosylation (15)
- Congenital Hyperinsulinism (50)
- Coproporphyria, Hereditary (13)
- Crigler-Najjar Syndrome (13)
- Cystinosis (35)
- DNA Repair-Deficiency Disorders (312)
- Deficiency Diseases (1,468)
- Dehydration (198)
- Diabetes Mellitus (19,417)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (3,219)
- Diabetes Mellitus, Type 2 (9,307)
- Diabetes, Gestational (696)
- Diabetic Ketoacidosis (68)
- Dihydropyrimidine Dehydrogenase Deficiency (1)
- Dyslipidemias (2,827)
- Fabry Disease (203)
- Familial Hypophosphatemic Rickets (59)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (99)
- Farber Lipogranulomatosis (2)
- Fetal Nutrition Disorders (4)
- Folic Acid Deficiency (26)
- Friedreich Ataxia (82)
- Frontotemporal Dementia (266)
- Frontotemporal Lobar Degeneration (255)
- Fructose Intolerance (12)
- Fructose Metabolism, Inborn Errors (12)
- Fructose-1,6-Diphosphatase Deficiency (1)
- Fucosidosis (9)
- Galactosemias (12)
- Gangliosidoses (38)
- Gangliosidoses, GM2 (25)
- Gangliosidosis, GM1 (18)
- Gaucher Disease (145)
- Gilbert Disease (2)
- Glucose Intolerance (1,237)
- Glucose Metabolism Disorders (16,530)
- Glucosephosphate Dehydrogenase Deficiency (49)
- Glycogen Storage Disease (190)
- Glycogen Storage Disease Type I (14)
- Glycogen Storage Disease Type II (146)
- Glycogen Storage Disease Type III (9)
- Glycogen Storage Disease Type IIb (3)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (16)
- Glycogen Storage Disease Type VI (3)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (3)
- Gout (311)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (27)
- Hemochromatosis (82)
- Hemosiderosis (82)
- Hepatic Encephalopathy (192)
- Hepatolenticular Degeneration (53)
- Hereditary Central Nervous System Demyelinating Diseases (102)
- Hermanski-Pudlak Syndrome (10)
- Holocarboxylase Synthetase Deficiency (4)
- Homocystinuria (14)
- Hyperargininemia (9)
- Hypercalcemia (60)
- Hypercholesterolemia (1,242)
- Hyperferritinemia (5)
- Hyperglycemia (1,432)
- Hyperglycinemia, Nonketotic (2)
- Hyperhomocysteinemia (48)
- Hyperinsulinism (3,010)
- Hyperkalemia (105)
- Hyperlactatemia (46)
- Hyperlipidemia, Familial Combined (43)
- Hyperlipidemias (2,060)
- Hyperlipoproteinemia Type I (26)
- Hyperlipoproteinemia Type II (214)
- Hyperlipoproteinemia Type III (7)
- Hyperlipoproteinemia Type IV (8)
- Hyperlipoproteinemia Type V (12)
- Hyperlipoproteinemias (2,022)
- Hypernatremia (45)
- Hyperoxaluria, Primary (42)
- Hyperphosphatemia (163)
- Hypertriglyceridemia (306)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (16)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (2)
- Hypobetalipoproteinemias (15)
- Hypocalcemia (151)
- Hypoglycemia (806)
- Hypokalemia (45)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (28)
- Hyponatremia (158)
- Hypophosphatasia (35)
- Hypophosphatemia (89)
- Hypophosphatemia, Familial (55)
- Ichthyosis, X-Linked (77)
- Immunoglobulin Light-chain Amyloidosis (187)
- Inappropriate ADH Syndrome (24)
- Infant Nutrition Disorders (49)
- Insulin Resistance (3,390)
- Iron Metabolism Disorders (811)
- Iron Overload (220)
- Kearns-Sayre Syndrome (9)
- Kernicterus (8)
- Ketosis (190)
- Kwashiorkor (36)
- Lactose Intolerance (45)
- Latent Autoimmune Diabetes in Adults (10)
- Lecithin Cholesterol Acyltransferase Deficiency (4)
- Leigh Disease (17)
- Lesch-Nyhan Syndrome (5)
- Leukodystrophy, Globoid Cell (27)
- Leukodystrophy, Metachromatic (44)
- Li-Fraumeni Syndrome (17)
- Lipid Metabolism Disorders (3,496)
- Lipid Metabolism, Inborn Errors (872)
- Lipidoses (527)
- Lipodystrophy (188)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (13)
- Lipomatosis (27)
- Lipomatosis, Multiple Symmetrical (27)
- Lysosomal Storage Diseases (858)
- MELAS Syndrome (20)
- MERRF Syndrome (2)
- Magnesium Deficiency (24)
- Malabsorption Syndromes (547)
- Malnutrition (2,970)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (8)
- Menkes Kinky Hair Syndrome (7)
- Metabolic Diseases (27,708)
- Metabolic Syndrome (1,847)
- Metabolism, Inborn Errors (2,557)
- Metal Metabolism, Inborn Errors (233)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (3)
- Mitochondrial Diseases (274)
- Mitochondrial Encephalomyopathies (27)
- Mitochondrial Myopathies (65)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (13)
- Mucopolysaccharidoses (215)
- Mucopolysaccharidosis I (68)
- Mucopolysaccharidosis II (73)
- Mucopolysaccharidosis III (45)
- Mucopolysaccharidosis IV (233)
- Mucopolysaccharidosis VI (34)
- Mucopolysaccharidosis VII (16)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (5)
- Multiple Carboxylase Deficiency (4)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (4)
- Nephrocalcinosis (17)
- Nesidioblastosis (50)
- Neuronal Ceroid-Lipofuscinoses (45)
- Niemann-Pick Disease, Type A (58)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (58)
- Niemann-Pick Diseases (58)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (7,473)
- Obesity (11,150)
- Obesity Hypoventilation Syndrome (58)
- Obesity, Abdominal (261)
- Obesity, Maternal (58)
- Obesity, Metabolically Benign (19)
- Obesity, Morbid (853)
- Oculocerebrorenal Syndrome (6)
- Ophthalmoplegia, Chronic Progressive External (12)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (37)
- Ornithine Carbamoyltransferase Deficiency Disease (28)
- Osteomalacia (48)
- Osteoporosis (1,598)
- Osteoporosis, Postmenopausal (321)
- Overnutrition (4,595)
- Paralysis, Hyperkalemic Periodic (4)
- Pediatric Obesity (989)
- Pelizaeus-Merzbacher Disease (7)
- Peroxisomal Disorders (69)
- Phenylketonuria, Maternal (4)
- Phenylketonurias (143)
- Phosphorus Metabolism Disorders (222)
- Piebaldism (5)
- Porphyria Cutanea Tarda (50)
- Porphyria, Acute Intermittent (20)
- Porphyria, Erythropoietic (59)
- Porphyria, Variegate (8)
- Porphyrias (59)
- Porphyrias, Hepatic (51)
- Potassium Deficiency (45)
- Prader-Willi Syndrome (120)
- Prediabetic State (1,007)
- Primary Progressive Nonfluent Aphasia (17)
- Progeria (9)
- Propionic Acidemia (22)
- Protein Deficiency (59)
- Protein-Energy Malnutrition (53)
- Proteostasis Deficiencies (1,425)
- Protoporphyria, Erythropoietic (22)
- Pseudohypoparathyroidism (17)
- Pseudopseudohypoparathyroidism (17)
- Purine-Pyrimidine Metabolism, Inborn Errors (194)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (5)
- Pyruvate Metabolism, Inborn Errors (32)
- Refeeding Syndrome (13)
- Refsum Disease (8)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (177)
- Riboflavin Deficiency (1)
- Rickets (210)
- Rickets, Hypophosphatemic (57)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (21)
- Scurvy (14)
- Severe Acute Malnutrition (96)
- Severe Combined Immunodeficiency (82)
- Shwachman-Diamond Syndrome (17)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (4)
- Skin Diseases, Metabolic (170)
- Smith-Lemli-Opitz Syndrome (17)
- Sphingolipidoses (447)
- Sprue, Tropical (9)
- Starvation (20)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (98)
- Sulfatidosis (36)
- Swayback (40)
- Synucleinopathies (3,570)
- TDP-43 Proteinopathies (934)
- Tangier Disease (5)
- Tay-Sachs Disease (27)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (354)
- Thiamine Deficiency (27)
- Tyrosinemias (16)
- Urea Cycle Disorders, Inborn (74)
- Vascular Calcification (86)
- Vitamin A Deficiency (66)
- Vitamin B 12 Deficiency (65)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (859)
- Vitamin E Deficiency (8)
- Vitamin K Deficiency (10)
- Wasting Syndrome (411)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (538)
- Werner Syndrome (3)
- Wernicke Encephalopathy (11)
- Whipple Disease (1)
- Wolfram Syndrome (11)
- Wolman Disease (34)
- Xanthomatosis (14)
- Xanthomatosis, Cerebrotendinous (11)
- Xeroderma Pigmentosum (14)
- Zellweger Syndrome (6)
- alpha-Mannosidosis (26)
- beta-Mannosidosis (1)