Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (5)
- Acid-Base Imbalance (196)
- Acidosis (220)
- Acidosis, Lactic (45)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (15)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (111)
- Adrenoleukodystrophy (50)
- Albinism (33)
- Albinism, Ocular (3)
- Albinism, Oculocutaneous (14)
- Alexander Disease (1)
- Alkalosis (22)
- Alkalosis, Respiratory (8)
- Alkaptonuria (7)
- Amino Acid Metabolism, Inborn Errors (264)
- Amyloid Neuropathies (29)
- Amyloid Neuropathies, Familial (27)
- Amyloidosis (597)
- Amyloidosis, Familial (43)
- Amyotrophic Lateral Sclerosis (675)
- Anemia, Iron-Deficiency (566)
- Anemia, Pernicious (3)
- Argininosuccinic Aciduria (5)
- Arthritis, Gouty (25)
- Ascorbic Acid Deficiency (10)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (29)
- Avitaminosis (827)
- Barth Syndrome (6)
- Beriberi (21)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (23)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,483)
- Brain Diseases, Metabolic (914)
- Brain Diseases, Metabolic, Inborn (764)
- CREST Syndrome (7)
- Calcinosis (260)
- Calciphylaxis (12)
- Calcium Metabolism Disorders (441)
- Canavan Disease (7)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (8)
- Carbohydrate Metabolism, Inborn Errors (463)
- Celiac Disease (240)
- Cerebral Amyloid Angiopathy (13)
- Cerebral Amyloid Angiopathy, Familial (13)
- Child Nutrition Disorders (70)
- Cholesterol Ester Storage Disease (27)
- Choline Deficiency (4)
- Chondrodysplasia Punctata, Rhizomelic (2)
- Chronic Kidney Disease-Mineral and Bone Disorder (41)
- Citrullinemia (8)
- Cockayne Syndrome (7)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (69)
- Congenital Disorders of Glycosylation (8)
- Congenital Hyperinsulinism (36)
- Coproporphyria, Hereditary (9)
- Crigler-Najjar Syndrome (12)
- Cystinosis (29)
- Cystinuria (19)
- DNA Repair-Deficiency Disorders (251)
- Deficiency Diseases (1,050)
- Dehydration (151)
- Dent Disease (9)
- Diabetes Mellitus (15,421)
- Diabetes Mellitus, Experimental (2)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,543)
- Diabetes Mellitus, Type 2 (7,464)
- Diabetes, Gestational (490)
- Diabetic Ketoacidosis (42)
- Dyslipidemias (2,372)
- Fabry Disease (158)
- Familial Hypophosphatemic Rickets (45)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (88)
- Fanconi Syndrome (97)
- Farber Lipogranulomatosis (2)
- Female Athlete Triad Syndrome (7)
- Fetal Nutrition Disorders (1)
- Folic Acid Deficiency (19)
- Friedreich Ataxia (62)
- Frontotemporal Dementia (179)
- Frontotemporal Lobar Degeneration (169)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (8)
- Gangliosidoses (29)
- Gangliosidoses, GM2 (20)
- Gangliosidosis, GM1 (13)
- Gaucher Disease (110)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (877)
- Glucose Metabolism Disorders (13,144)
- Glucosephosphate Dehydrogenase Deficiency (42)
- Glycogen Storage Disease (142)
- Glycogen Storage Disease Type I (11)
- Glycogen Storage Disease Type II (108)
- Glycogen Storage Disease Type III (6)
- Glycogen Storage Disease Type IIb (2)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (13)
- Glycogen Storage Disease Type VI (2)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (2)
- Gout (229)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (24)
- Hemochromatosis (49)
- Hemosiderosis (28)
- Hepatic Encephalopathy (149)
- Hepatolenticular Degeneration (26)
- Hereditary Central Nervous System Demyelinating Diseases (81)
- Hermanski-Pudlak Syndrome (8)
- Homocystinuria (9)
- Hyperargininemia (4)
- Hypercalcemia (54)
- Hypercholesterolemia (1,055)
- Hyperglycemia (1,101)
- Hyperhomocysteinemia (42)
- Hyperinsulinism (2,478)
- Hyperkalemia (63)
- Hyperlactatemia (27)
- Hyperlipidemia, Familial Combined (37)
- Hyperlipidemias (1,743)
- Hyperlipoproteinemia Type I (21)
- Hyperlipoproteinemia Type II (158)
- Hyperlipoproteinemia Type III (5)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (9)
- Hyperlipoproteinemias (1,711)
- Hypernatremia (33)
- Hyperoxaluria, Primary (34)
- Hyperphosphatemia (141)
- Hypertriglyceridemia (264)
- Hypertriglyceridemic Waist (5)
- Hypervitaminosis A (2)
- Hypoalphalipoproteinemias (15)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (12)
- Hypocalcemia (113)
- Hypoglycemia (643)
- Hypokalemia (33)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (25)
- Hyponatremia (133)
- Hypophosphatasia (29)
- Hypophosphatemia (66)
- Hypophosphatemia, Familial (42)
- Ichthyosis, X-Linked (59)
- Immunoglobulin Light-chain Amyloidosis (159)
- Inappropriate ADH Syndrome (20)
- Infant Nutrition Disorders (34)
- Insulin Resistance (2,816)
- Iron Metabolism Disorders (645)
- Iron Overload (200)
- Kearns-Sayre Syndrome (7)
- Kernicterus (7)
- Ketosis (100)
- Kwashiorkor (22)
- Lactose Intolerance (36)
- Latent Autoimmune Diabetes in Adults (8)
- Lecithin Cholesterol Acyltransferase Deficiency (3)
- Leigh Disease (11)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (23)
- Leukodystrophy, Metachromatic (36)
- Li-Fraumeni Syndrome (13)
- Liddle Syndrome (1)
- Lipid Metabolism Disorders (2,866)
- Lipid Metabolism, Inborn Errors (681)
- Lipidoses (409)
- Lipodystrophy (163)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (10)
- Lipomatosis (7)
- Lipomatosis, Multiple Symmetrical (7)
- Lysosomal Storage Diseases (685)
- MELAS Syndrome (14)
- Magnesium Deficiency (19)
- Malabsorption Syndromes (412)
- Malnutrition (2,326)
- Mannosidase Deficiency Diseases (25)
- Maple Syrup Urine Disease (3)
- Menkes Kinky Hair Syndrome (3)
- Metabolic Diseases (21,865)
- Metabolic Syndrome (1,507)
- Metabolism, Inborn Errors (2,044)
- Metal Metabolism, Inborn Errors (161)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (1)
- Mitochondrial Diseases (199)
- Mitochondrial Encephalomyopathies (19)
- Mitochondrial Myopathies (38)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (11)
- Mucopolysaccharidoses (170)
- Mucopolysaccharidosis I (57)
- Mucopolysaccharidosis II (51)
- Mucopolysaccharidosis III (37)
- Mucopolysaccharidosis IV (180)
- Mucopolysaccharidosis VI (28)
- Mucopolysaccharidosis VII (12)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (3)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (2)
- Nephrocalcinosis (9)
- Nesidioblastosis (1)
- Neuronal Ceroid-Lipofuscinoses (30)
- Niemann-Pick Disease, Type A (49)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (49)
- Niemann-Pick Diseases (49)
- Nutrition Disorders (5,626)
- Obesity (8,598)
- Obesity Hypoventilation Syndrome (45)
- Obesity, Abdominal (189)
- Obesity, Metabolically Benign (10)
- Obesity, Morbid (636)
- Oculocerebrorenal Syndrome (5)
- Ophthalmoplegia, Chronic Progressive External (8)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (30)
- Ornithine Carbamoyltransferase Deficiency Disease (17)
- Osteomalacia (40)
- Osteoporosis (1,344)
- Osteoporosis, Postmenopausal (255)
- Overnutrition (3,388)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (717)
- Pelizaeus-Merzbacher Disease (5)
- Peroxisomal Disorders (55)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (108)
- Phosphorus Metabolism Disorders (181)
- Piebaldism (4)
- Porphyria Cutanea Tarda (38)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (46)
- Porphyria, Variegate (7)
- Porphyrias (46)
- Porphyrias, Hepatic (38)
- Potassium Deficiency (33)
- Prader-Willi Syndrome (93)
- Prediabetic State (674)
- Primary Progressive Nonfluent Aphasia (13)
- Progeria (8)
- Propionic Acidemia (12)
- Protein Deficiency (35)
- Protein-Energy Malnutrition (40)
- Protoporphyria, Erythropoietic (15)
- Pseudohypoaldosteronism (5)
- Pseudohypoparathyroidism (13)
- Pseudopseudohypoparathyroidism (13)
- Purine-Pyrimidine Metabolism, Inborn Errors (139)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (3)
- Pyruvate Metabolism, Inborn Errors (20)
- Refeeding Syndrome (9)
- Refsum Disease (7)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (152)
- Rickets (168)
- Rickets, Hypophosphatemic (44)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (17)
- Scurvy (9)
- Severe Acute Malnutrition (63)
- Severe Combined Immunodeficiency (71)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (143)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (349)
- Sprue, Tropical (8)
- Starvation (17)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (72)
- Sulfatidosis (31)
- Swayback (18)
- TDP-43 Proteinopathies (667)
- Tangier Disease (5)
- Tay-Sachs Disease (22)
- Tetany (327)
- Thiamine Deficiency (21)
- Tyrosinemias (12)
- Urea Cycle Disorders, Inborn (59)
- Vascular Calcification (69)
- Vitamin A Deficiency (54)
- Vitamin B 12 Deficiency (46)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (684)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (6)
- Wasting Syndrome (314)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (402)
- Werner Syndrome (1)
- Wernicke Encephalopathy (8)
- Whipple Disease (1)
- Wolfram Syndrome (8)
- Wolman Disease (28)
- Xanthomatosis (10)
- Xanthomatosis, Cerebrotendinous (8)
- Xeroderma Pigmentosum (10)
- Zellweger Syndrome (5)
- alpha-Mannosidosis (25)
- beta-Mannosidosis (1)