Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (4)
- Achlorhydria (6)
- Acid-Base Imbalance (307)
- Acidosis (332)
- Acidosis, Lactic (54)
- Acidosis, Renal Tubular (10)
- Acidosis, Respiratory (20)
- Adiposis Dolorosa (6)
- Adrenal Hyperplasia, Congenital (148)
- Adrenoleukodystrophy (67)
- Albinism (40)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (15)
- Alexander Disease (4)
- Alkalosis (28)
- Alkalosis, Respiratory (8)
- Alkaptonuria (9)
- Amino Acid Metabolism, Inborn Errors (345)
- Amyloid Neuropathies (53)
- Amyloid Neuropathies, Familial (47)
- Amyloidosis (872)
- Amyloidosis, Familial (84)
- Amyotrophic Lateral Sclerosis (1,003)
- Anemia, Iron-Deficiency (782)
- Anemia, Pernicious (5)
- Argininosuccinic Aciduria (10)
- Arthritis, Gouty (48)
- Ascorbic Acid Deficiency (16)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (47)
- Avitaminosis (1,067)
- Barth Syndrome (8)
- Beriberi (27)
- Biotinidase Deficiency (6)
- Blind Loop Syndrome (35)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (8)
- Bone Diseases, Metabolic (1,853)
- Brain Diseases, Metabolic (1,252)
- Brain Diseases, Metabolic, Inborn (1,046)
- CREST Syndrome (9)
- Calcinosis (378)
- Calcinosis Cutis (6)
- Calciphylaxis (17)
- Calcium Metabolism Disorders (594)
- Canavan Disease (10)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (10)
- Carbohydrate Metabolism, Inborn Errors (622)
- Celiac Disease (337)
- Cerebral Amyloid Angiopathy (28)
- Cerebral Amyloid Angiopathy, Familial (28)
- Child Nutrition Disorders (125)
- Cholesterol Ester Storage Disease (33)
- Choline Deficiency (5)
- Chondrodysplasia Punctata, Rhizomelic (4)
- Chronic Kidney Disease-Mineral and Bone Disorder (54)
- Citrullinemia (13)
- Cockayne Syndrome (10)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (96)
- Congenital Disorders of Glycosylation (14)
- Congenital Hyperinsulinism (50)
- Coproporphyria, Hereditary (13)
- Crigler-Najjar Syndrome (13)
- Cystinosis (40)
- DNA Repair-Deficiency Disorders (321)
- Deficiency Diseases (1,511)
- Dehydration (207)
- Diabetes Mellitus (20,139)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (3,341)
- Diabetes Mellitus, Type 2 (9,631)
- Diabetes, Gestational (732)
- Diabetic Ketoacidosis (72)
- Dihydropyrimidine Dehydrogenase Deficiency (1)
- Dyslipidemias (2,897)
- Fabry Disease (212)
- Familial Hypophosphatemic Rickets (62)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (104)
- Farber Lipogranulomatosis (2)
- Fetal Nutrition Disorders (4)
- Folic Acid Deficiency (29)
- Friedreich Ataxia (86)
- Frontotemporal Dementia (287)
- Frontotemporal Lobar Degeneration (271)
- Fructose Intolerance (14)
- Fructose Metabolism, Inborn Errors (14)
- Fructose-1,6-Diphosphatase Deficiency (1)
- Fucosidosis (9)
- Galactosemias (12)
- Gangliosidoses (38)
- Gangliosidoses, GM2 (25)
- Gangliosidosis, GM1 (18)
- Gaucher Disease (149)
- Gilbert Disease (2)
- Glucose Intolerance (1,290)
- Glucose Metabolism Disorders (17,083)
- Glucosephosphate Dehydrogenase Deficiency (51)
- Glycogen Storage Disease (197)
- Glycogen Storage Disease Type I (15)
- Glycogen Storage Disease Type II (150)
- Glycogen Storage Disease Type III (9)
- Glycogen Storage Disease Type IIb (4)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (17)
- Glycogen Storage Disease Type VI (3)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (4)
- Gout (321)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (27)
- Hemochromatosis (84)
- Hemosiderosis (84)
- Hepatic Encephalopathy (198)
- Hepatolenticular Degeneration (56)
- Hereditary Central Nervous System Demyelinating Diseases (105)
- Hermanski-Pudlak Syndrome (10)
- Holocarboxylase Synthetase Deficiency (5)
- Homocystinuria (15)
- Homozygous Familial Hypercholesterolemia (67)
- Hyperargininemia (11)
- Hypercalcemia (60)
- Hypercholesterolemia (1,263)
- Hyperferritinemia (5)
- Hyperglycemia (1,495)
- Hyperglycinemia, Nonketotic (3)
- Hyperhomocysteinemia (49)
- Hyperinsulinism (3,110)
- Hyperkalemia (109)
- Hyperlactatemia (47)
- Hyperlipidemia, Familial Combined (43)
- Hyperlipidemias (2,107)
- Hyperlipoproteinemia Type I (27)
- Hyperlipoproteinemia Type II (220)
- Hyperlipoproteinemia Type III (7)
- Hyperlipoproteinemia Type IV (9)
- Hyperlipoproteinemia Type V (12)
- Hyperlipoproteinemias (2,069)
- Hypernatremia (47)
- Hyperoxaluria, Primary (44)
- Hyperphosphatemia (164)
- Hypertriglyceridemia (316)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (16)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (2)
- Hypobetalipoproteinemias (15)
- Hypocalcemia (158)
- Hypoglycemia (826)
- Hypokalemia (46)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (28)
- Hyponatremia (164)
- Hypophosphatasia (40)
- Hypophosphatemia (96)
- Hypophosphatemia, Familial (58)
- Ichthyosis, X-Linked (81)
- Immunoglobulin Light-chain Amyloidosis (193)
- Inappropriate ADH Syndrome (25)
- Infant Nutrition Disorders (53)
- Insulin Resistance (3,500)
- Iron Deficiencies (782)
- Iron Metabolism Disorders (913)
- Iron Overload (222)
- Kearns-Sayre Syndrome (9)
- Kernicterus (9)
- Ketosis (208)
- Kwashiorkor (40)
- Lactose Intolerance (46)
- Latent Autoimmune Diabetes in Adults (11)
- Lecithin Cholesterol Acyltransferase Deficiency (4)
- Leigh Disease (17)
- Lesch-Nyhan Syndrome (5)
- Leukodystrophy, Globoid Cell (27)
- Leukodystrophy, Metachromatic (44)
- Li-Fraumeni Syndrome (18)
- Lipid Metabolism Disorders (3,602)
- Lipid Metabolism, Inborn Errors (926)
- Lipidoses (543)
- Lipodystrophy (192)
- Lipodystrophy, Congenital Generalized (10)
- Lipodystrophy, Familial Partial (15)
- Lipomatosis (28)
- Lipomatosis, Multiple Symmetrical (28)
- Lysosomal Storage Diseases (888)
- MELAS Syndrome (20)
- MERRF Syndrome (3)
- Magnesium Deficiency (24)
- Malabsorption Syndromes (566)
- Malnutrition (3,099)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (9)
- Menkes Kinky Hair Syndrome (7)
- Metabolic Diseases (28,794)
- Metabolic Syndrome (1,908)
- Metabolism, Inborn Errors (2,681)
- Metal Metabolism, Inborn Errors (247)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (3)
- Mitochondrial Diseases (291)
- Mitochondrial Encephalomyopathies (28)
- Mitochondrial Myopathies (71)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (13)
- Mucopolysaccharidoses (222)
- Mucopolysaccharidosis I (70)
- Mucopolysaccharidosis II (77)
- Mucopolysaccharidosis III (47)
- Mucopolysaccharidosis IV (252)
- Mucopolysaccharidosis VI (35)
- Mucopolysaccharidosis VII (17)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (6)
- Multiple Carboxylase Deficiency (5)
- Multiple Sulfatase Deficiency Disease (2)
- Necrobiosis Lipoidica (4)
- Nephrocalcinosis (18)
- Nesidioblastosis (50)
- Neuronal Ceroid-Lipofuscinoses (45)
- Niemann-Pick Disease, Type A (61)
- Niemann-Pick Disease, Type B (3)
- Niemann-Pick Disease, Type C (61)
- Niemann-Pick Diseases (61)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (9,678)
- Obesity (11,620)
- Obesity Hypoventilation Syndrome (60)
- Obesity, Abdominal (277)
- Obesity, Maternal (60)
- Obesity, Metabolically Benign (20)
- Obesity, Morbid (889)
- Oculocerebrorenal Syndrome (7)
- Ophthalmoplegia, Chronic Progressive External (12)
- Optic Atrophy, Autosomal Dominant (7)
- Optic Atrophy, Hereditary, Leber (37)
- Ornithine Carbamoyltransferase Deficiency Disease (29)
- Osteomalacia (48)
- Osteoporosis (1,641)
- Osteoporosis, Postmenopausal (324)
- Overnutrition (6,708)
- Overweight (7,235)
- Paralysis, Hyperkalemic Periodic (4)
- Pediatric Obesity (1,036)
- Pelizaeus-Merzbacher Disease (7)
- Peroxisomal Disorders (75)
- Phenylketonuria, Maternal (4)
- Phenylketonurias (150)
- Phosphorus Metabolism Disorders (229)
- Piebaldism (5)
- Porphyria Cutanea Tarda (52)
- Porphyria, Acute Intermittent (21)
- Porphyria, Erythropoietic (61)
- Porphyria, Variegate (8)
- Porphyrias (61)
- Porphyrias, Hepatic (53)
- Potassium Deficiency (46)
- Prader-Willi Syndrome (124)
- Prediabetic State (1,058)
- Primary Progressive Nonfluent Aphasia (17)
- Progeria (10)
- Propionic Acidemia (21)
- Protein Deficiency (62)
- Protein-Energy Malnutrition (55)
- Proteostasis Deficiencies (1,502)
- Protoporphyria, Erythropoietic (23)
- Pseudohypoparathyroidism (18)
- Pseudopseudohypoparathyroidism (18)
- Purine-Pyrimidine Metabolism, Inborn Errors (203)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (5)
- Pyruvate Metabolism, Inborn Errors (32)
- Refeeding Syndrome (15)
- Refsum Disease (9)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (185)
- Riboflavin Deficiency (1)
- Rickets (217)
- Rickets, Hypophosphatemic (60)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (21)
- Scurvy (14)
- Severe Acute Malnutrition (109)
- Severe Combined Immunodeficiency (83)
- Shwachman-Diamond Syndrome (18)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (4)
- Skin Diseases, Metabolic (173)
- Smith-Lemli-Opitz Syndrome (17)
- Sphingolipidoses (463)
- Sprue, Tropical (9)
- Starvation (22)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (102)
- Sulfatidosis (37)
- Swayback (44)
- Synucleinopathies (3,757)
- TDP-43 Proteinopathies (981)
- Tangier Disease (5)
- Tay-Sachs Disease (27)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (364)
- Thiamine Deficiency (27)
- Tyrosinemias (17)
- Urea Cycle Disorders, Inborn (76)
- Vascular Calcification (88)
- Vitamin A Deficiency (69)
- Vitamin B 12 Deficiency (69)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (883)
- Vitamin E Deficiency (8)
- Vitamin K Deficiency (11)
- Wasting Syndrome (430)
- Water Intoxication (13)
- Water-Electrolyte Imbalance (568)
- 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)