Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (4)
- Achlorhydria (6)
- Acid-Base Imbalance (281)
- Acidosis (303)
- Acidosis, Lactic (52)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (18)
- Adiposis Dolorosa (6)
- Adrenal Hyperplasia, Congenital (142)
- Adrenoleukodystrophy (63)
- Albinism (36)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (4)
- Alkalosis (25)
- Alkalosis, Respiratory (8)
- Alkaptonuria (9)
- Amino Acid Metabolism, Inborn Errors (325)
- Amyloid Neuropathies (49)
- Amyloid Neuropathies, Familial (43)
- Amyloidosis (792)
- Amyloidosis, Familial (72)
- Amyotrophic Lateral Sclerosis (917)
- Anemia, Iron-Deficiency (725)
- Anemia, Pernicious (5)
- Argininosuccinic Aciduria (9)
- Arthritis, Gouty (40)
- Ascorbic Acid Deficiency (15)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (46)
- Avitaminosis (1,013)
- Barth Syndrome (8)
- Beriberi (27)
- Biotinidase Deficiency (5)
- Blind Loop Syndrome (32)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,760)
- Brain Diseases, Metabolic (1,171)
- Brain Diseases, Metabolic, Inborn (983)
- CREST Syndrome (9)
- Calcinosis (344)
- Calciphylaxis (16)
- Calcium Metabolism Disorders (564)
- Canavan Disease (10)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (9)
- Carbohydrate Metabolism, Inborn Errors (591)
- Celiac Disease (316)
- Cerebral Amyloid Angiopathy (24)
- Cerebral Amyloid Angiopathy, Familial (24)
- Child Nutrition Disorders (111)
- Cholesterol Ester Storage Disease (33)
- Choline Deficiency (5)
- Chondrodysplasia Punctata, Rhizomelic (3)
- Chronic Kidney Disease-Mineral and Bone Disorder (52)
- Citrullinemia (12)
- Cockayne Syndrome (10)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (92)
- Congenital Disorders of Glycosylation (15)
- Congenital Hyperinsulinism (50)
- Coproporphyria, Hereditary (13)
- Crigler-Najjar Syndrome (13)
- Cystinosis (34)
- DNA Repair-Deficiency Disorders (310)
- Deficiency Diseases (1,433)
- Dehydration (193)
- Diabetes Mellitus (18,989)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (3,149)
- Diabetes Mellitus, Type 2 (9,108)
- Diabetes, Gestational (677)
- Diabetic Ketoacidosis (66)
- Dihydropyrimidine Dehydrogenase Deficiency (1)
- Dyslipidemias (2,774)
- Fabry Disease (196)
- Familial Hypophosphatemic Rickets (58)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (99)
- Farber Lipogranulomatosis (2)
- Fetal Nutrition Disorders (4)
- Folic Acid Deficiency (25)
- Friedreich Ataxia (82)
- Frontotemporal Dementia (254)
- Frontotemporal Lobar Degeneration (243)
- Fructose Intolerance (12)
- Fructose Metabolism, Inborn Errors (12)
- Fructose-1,6-Diphosphatase Deficiency (1)
- Fucosidosis (9)
- Galactosemias (12)
- Gangliosidoses (37)
- Gangliosidoses, GM2 (24)
- Gangliosidosis, GM1 (18)
- Gaucher Disease (141)
- Gilbert Disease (2)
- Glucose Intolerance (1,211)
- Glucose Metabolism Disorders (16,177)
- Glucosephosphate Dehydrogenase Deficiency (48)
- Glycogen Storage Disease (188)
- Glycogen Storage Disease Type I (14)
- Glycogen Storage Disease Type II (144)
- 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 (305)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (27)
- Hemochromatosis (80)
- Hemosiderosis (80)
- Hepatic Encephalopathy (187)
- Hepatolenticular Degeneration (51)
- Hereditary Central Nervous System Demyelinating Diseases (99)
- Hermanski-Pudlak Syndrome (10)
- Holocarboxylase Synthetase Deficiency (4)
- Homocystinuria (13)
- Hyperargininemia (9)
- Hypercalcemia (60)
- Hypercholesterolemia (1,221)
- Hyperferritinemia (4)
- Hyperglycemia (1,402)
- Hyperglycinemia, Nonketotic (2)
- Hyperhomocysteinemia (46)
- Hyperinsulinism (2,943)
- Hyperkalemia (102)
- Hyperlactatemia (45)
- Hyperlipidemia, Familial Combined (42)
- Hyperlipidemias (2,020)
- Hyperlipoproteinemia Type I (26)
- Hyperlipoproteinemia Type II (206)
- Hyperlipoproteinemia Type III (7)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (12)
- Hyperlipoproteinemias (1,983)
- Hypernatremia (43)
- Hyperoxaluria, Primary (41)
- Hyperphosphatemia (161)
- Hypertriglyceridemia (301)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (16)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (2)
- Hypobetalipoproteinemias (15)
- Hypocalcemia (148)
- Hypoglycemia (792)
- Hypokalemia (43)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (28)
- Hyponatremia (157)
- Hypophosphatasia (35)
- Hypophosphatemia (88)
- Hypophosphatemia, Familial (54)
- Ichthyosis, X-Linked (73)
- Immunoglobulin Light-chain Amyloidosis (185)
- Inappropriate ADH Syndrome (24)
- Infant Nutrition Disorders (46)
- Insulin Resistance (3,318)
- Iron Metabolism Disorders (796)
- Iron Overload (217)
- Kearns-Sayre Syndrome (9)
- Kernicterus (8)
- Ketosis (184)
- 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 (26)
- Leukodystrophy, Metachromatic (43)
- Li-Fraumeni Syndrome (17)
- Lipid Metabolism Disorders (3,424)
- Lipid Metabolism, Inborn Errors (849)
- Lipidoses (513)
- Lipodystrophy (186)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (13)
- Lipomatosis (25)
- Lipomatosis, Multiple Symmetrical (25)
- Lysosomal Storage Diseases (836)
- MELAS Syndrome (20)
- MERRF Syndrome (2)
- Magnesium Deficiency (24)
- Malabsorption Syndromes (537)
- Malnutrition (2,893)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (6)
- Menkes Kinky Hair Syndrome (7)
- Metabolic Diseases (27,093)
- Metabolic Syndrome (1,801)
- Metabolism, Inborn Errors (2,496)
- Metal Metabolism, Inborn Errors (228)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (3)
- Mitochondrial Diseases (272)
- Mitochondrial Encephalomyopathies (26)
- Mitochondrial Myopathies (64)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (12)
- Mucopolysaccharidoses (210)
- Mucopolysaccharidosis I (68)
- Mucopolysaccharidosis II (72)
- Mucopolysaccharidosis III (43)
- Mucopolysaccharidosis IV (228)
- Mucopolysaccharidosis VI (33)
- Mucopolysaccharidosis VII (16)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (5)
- Multiple Carboxylase Deficiency (4)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (4)
- Nephrocalcinosis (16)
- Nesidioblastosis (50)
- Neuronal Ceroid-Lipofuscinoses (44)
- Niemann-Pick Disease, Type A (57)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (57)
- Niemann-Pick Diseases (57)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (7,232)
- Obesity (10,824)
- Obesity Hypoventilation Syndrome (57)
- Obesity, Abdominal (248)
- Obesity, Maternal (57)
- Obesity, Metabolically Benign (19)
- Obesity, Morbid (827)
- Oculocerebrorenal Syndrome (6)
- Ophthalmoplegia, Chronic Progressive External (12)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (35)
- Ornithine Carbamoyltransferase Deficiency Disease (28)
- Osteomalacia (47)
- Osteoporosis (1,564)
- Osteoporosis, Postmenopausal (319)
- Overnutrition (4,428)
- Paralysis, Hyperkalemic Periodic (4)
- Pediatric Obesity (953)
- Pelizaeus-Merzbacher Disease (7)
- Peroxisomal Disorders (68)
- Phenylketonuria, Maternal (4)
- Phenylketonurias (139)
- Phosphorus Metabolism Disorders (218)
- Piebaldism (5)
- Porphyria Cutanea Tarda (48)
- Porphyria, Acute Intermittent (20)
- Porphyria, Erythropoietic (57)
- Porphyria, Variegate (7)
- Porphyrias (57)
- Porphyrias, Hepatic (49)
- Potassium Deficiency (43)
- Prader-Willi Syndrome (115)
- Prediabetic State (979)
- Primary Progressive Nonfluent Aphasia (17)
- Progeria (9)
- Propionic Acidemia (20)
- Protein Deficiency (57)
- Protein-Energy Malnutrition (52)
- Proteostasis Deficiencies (1,366)
- Protoporphyria, Erythropoietic (21)
- Pseudohypoparathyroidism (17)
- Pseudopseudohypoparathyroidism (17)
- Purine-Pyrimidine Metabolism, Inborn Errors (189)
- 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 (176)
- Riboflavin Deficiency (1)
- Rickets (207)
- Rickets, Hypophosphatemic (56)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (21)
- Scurvy (13)
- Severe Acute Malnutrition (95)
- Severe Combined Immunodeficiency (82)
- Shwachman-Diamond Syndrome (17)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (4)
- Skin Diseases, Metabolic (168)
- Smith-Lemli-Opitz Syndrome (17)
- Sphingolipidoses (434)
- Sprue, Tropical (9)
- Starvation (19)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (98)
- Sulfatidosis (35)
- Swayback (35)
- Synucleinopathies (3,441)
- TDP-43 Proteinopathies (901)
- Tangier Disease (5)
- Tay-Sachs Disease (26)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (352)
- Thiamine Deficiency (27)
- Tyrosinemias (15)
- Urea Cycle Disorders, Inborn (73)
- Vascular Calcification (83)
- Vitamin A Deficiency (64)
- Vitamin B 12 Deficiency (62)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (843)
- Vitamin E Deficiency (8)
- Vitamin K Deficiency (9)
- Wasting Syndrome (402)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (525)
- Werner Syndrome (2)
- 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)