Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (6)
- Acid-Base Imbalance (232)
- Acidosis (251)
- Acidosis, Lactic (50)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (17)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (127)
- Adrenoleukodystrophy (56)
- Albinism (35)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (3)
- Alkalosis (24)
- Alkalosis, Respiratory (8)
- Alkaptonuria (9)
- Amino Acid Metabolism, Inborn Errors (294)
- Amyloid Neuropathies (39)
- Amyloid Neuropathies, Familial (35)
- Amyloidosis (689)
- Amyloidosis, Familial (55)
- Amyotrophic Lateral Sclerosis (792)
- Anemia, Iron-Deficiency (644)
- Anemia, Pernicious (3)
- Argininosuccinic Aciduria (8)
- Arthritis, Gouty (29)
- Ascorbic Acid Deficiency (11)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (36)
- Avitaminosis (916)
- Barth Syndrome (6)
- Beriberi (23)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (30)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,615)
- Brain Diseases, Metabolic (1,043)
- Brain Diseases, Metabolic, Inborn (878)
- CREST Syndrome (9)
- Calcinosis (302)
- Calciphylaxis (14)
- Calcium Metabolism Disorders (504)
- Canavan Disease (8)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (8)
- Carbohydrate Metabolism, Inborn Errors (518)
- Celiac Disease (272)
- Cerebral Amyloid Angiopathy (17)
- Cerebral Amyloid Angiopathy, Familial (17)
- Child Nutrition Disorders (87)
- Cholesterol Ester Storage Disease (29)
- Choline Deficiency (4)
- Chondrodysplasia Punctata, Rhizomelic (3)
- Chronic Kidney Disease-Mineral and Bone Disorder (47)
- Citrullinemia (11)
- Cockayne Syndrome (7)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (82)
- Congenital Disorders of Glycosylation (9)
- Congenital Hyperinsulinism (47)
- Coproporphyria, Hereditary (11)
- Crigler-Najjar Syndrome (12)
- Cystinosis (29)
- Cystinuria (20)
- DNA Repair-Deficiency Disorders (281)
- Deficiency Diseases (1,169)
- Dehydration (169)
- Dent Disease (10)
- Diabetes Mellitus (17,022)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,833)
- Diabetes Mellitus, Type 2 (8,199)
- Diabetes, Gestational (570)
- Diabetic Ketoacidosis (51)
- Dyslipidemias (2,562)
- Fabry Disease (178)
- Familial Hypophosphatemic Rickets (54)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (94)
- Fanconi Syndrome (103)
- Farber Lipogranulomatosis (2)
- Female Athlete Triad Syndrome (9)
- Fetal Nutrition Disorders (3)
- Folic Acid Deficiency (21)
- Friedreich Ataxia (73)
- Frontotemporal Dementia (219)
- Frontotemporal Lobar Degeneration (208)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (10)
- Gangliosidoses (35)
- Gangliosidoses, GM2 (24)
- Gangliosidosis, GM1 (17)
- Gaucher Disease (127)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (1,026)
- Glucose Metabolism Disorders (14,580)
- Glucosephosphate Dehydrogenase Deficiency (43)
- Glycogen Storage Disease (166)
- Glycogen Storage Disease Type I (12)
- Glycogen Storage Disease Type II (122)
- Glycogen Storage Disease Type III (7)
- Glycogen Storage Disease Type IIb (2)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (16)
- Glycogen Storage Disease Type VI (2)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (2)
- Gout (267)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (26)
- Hemochromatosis (50)
- Hemosiderosis (28)
- Hepatic Encephalopathy (165)
- Hepatolenticular Degeneration (40)
- Hereditary Central Nervous System Demyelinating Diseases (89)
- Hermanski-Pudlak Syndrome (9)
- Homocystinuria (10)
- Hyperargininemia (7)
- Hypercalcemia (56)
- Hypercholesterolemia (1,138)
- Hyperglycemia (1,272)
- Hyperhomocysteinemia (43)
- Hyperinsulinism (2,702)
- Hyperkalemia (79)
- Hyperlactatemia (36)
- Hyperlipidemia, Familial Combined (38)
- Hyperlipidemias (1,878)
- Hyperlipoproteinemia Type I (22)
- Hyperlipoproteinemia Type II (184)
- Hyperlipoproteinemia Type III (6)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (10)
- Hyperlipoproteinemias (1,841)
- Hypernatremia (38)
- Hyperoxaluria, Primary (37)
- Hyperphosphatemia (156)
- Hypertriglyceridemia (278)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (15)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (12)
- Hypocalcemia (130)
- Hypoglycemia (725)
- Hypokalemia (38)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (25)
- Hyponatremia (147)
- Hypophosphatasia (30)
- Hypophosphatemia (80)
- Hypophosphatemia, Familial (51)
- Ichthyosis, X-Linked (65)
- Immunoglobulin Light-chain Amyloidosis (174)
- Inappropriate ADH Syndrome (22)
- Infant Nutrition Disorders (39)
- Insulin Resistance (3,065)
- Iron Metabolism Disorders (717)
- Iron Overload (209)
- Kearns-Sayre Syndrome (7)
- Kernicterus (8)
- Ketosis (136)
- Kwashiorkor (27)
- Lactose Intolerance (37)
- Latent Autoimmune Diabetes in Adults (8)
- Lecithin Cholesterol Acyltransferase Deficiency (4)
- Leigh Disease (14)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (26)
- Leukodystrophy, Metachromatic (40)
- Li-Fraumeni Syndrome (15)
- Liddle Syndrome (1)
- Lipid Metabolism Disorders (3,132)
- Lipid Metabolism, Inborn Errors (769)
- Lipidoses (469)
- Lipodystrophy (174)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (11)
- Lipomatosis (10)
- Lipomatosis, Multiple Symmetrical (10)
- Lysosomal Storage Diseases (763)
- MELAS Syndrome (17)
- Magnesium Deficiency (21)
- Malabsorption Syndromes (466)
- Malnutrition (2,595)
- Mannosidase Deficiency Diseases (27)
- Maple Syrup Urine Disease (5)
- Menkes Kinky Hair Syndrome (4)
- Metabolic Diseases (24,365)
- Metabolic Syndrome (1,644)
- Metabolism, Inborn Errors (2,306)
- Metal Metabolism, Inborn Errors (190)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (3)
- Mitochondrial Diseases (237)
- Mitochondrial Encephalomyopathies (23)
- Mitochondrial Myopathies (48)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (12)
- Mucopolysaccharidoses (186)
- Mucopolysaccharidosis I (62)
- Mucopolysaccharidosis II (60)
- Mucopolysaccharidosis III (39)
- Mucopolysaccharidosis IV (197)
- Mucopolysaccharidosis VI (29)
- Mucopolysaccharidosis VII (13)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (4)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (4)
- Nephrocalcinosis (13)
- Nesidioblastosis (1)
- Neuronal Ceroid-Lipofuscinoses (38)
- Niemann-Pick Disease, Type A (52)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (52)
- Niemann-Pick Diseases (52)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (6,380)
- Obesity (9,672)
- Obesity Hypoventilation Syndrome (53)
- Obesity, Abdominal (221)
- Obesity, Metabolically Benign (14)
- Obesity, Morbid (741)
- Oculocerebrorenal Syndrome (6)
- Ophthalmoplegia, Chronic Progressive External (9)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (34)
- Ornithine Carbamoyltransferase Deficiency Disease (24)
- Osteomalacia (44)
- Osteoporosis (1,444)
- Osteoporosis, Postmenopausal (284)
- Overnutrition (3,871)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (829)
- Pelizaeus-Merzbacher Disease (6)
- Peroxisomal Disorders (62)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (123)
- Phosphorus Metabolism Disorders (208)
- Piebaldism (4)
- Porphyria Cutanea Tarda (42)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (50)
- Porphyria, Variegate (7)
- Porphyrias (50)
- Porphyrias, Hepatic (42)
- Potassium Deficiency (38)
- Prader-Willi Syndrome (102)
- Prediabetic State (803)
- Primary Progressive Nonfluent Aphasia (16)
- Progeria (9)
- Propionic Acidemia (13)
- Protein Deficiency (45)
- Protein-Energy Malnutrition (46)
- Proteostasis Deficiencies (1,166)
- Protoporphyria, Erythropoietic (17)
- Pseudohypoaldosteronism (5)
- Pseudohypoparathyroidism (17)
- Pseudopseudohypoparathyroidism (17)
- Purine-Pyrimidine Metabolism, Inborn Errors (161)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (4)
- Pyruvate Metabolism, Inborn Errors (26)
- Refeeding Syndrome (11)
- Refsum Disease (8)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (167)
- Rickets (187)
- Rickets, Hypophosphatemic (53)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (21)
- Scurvy (10)
- Severe Acute Malnutrition (75)
- Severe Combined Immunodeficiency (78)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (156)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (397)
- Sprue, Tropical (8)
- Starvation (17)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (85)
- Sulfatidosis (33)
- Swayback (21)
- TDP-43 Proteinopathies (792)
- Tangier Disease (5)
- Tay-Sachs Disease (26)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (338)
- Thiamine Deficiency (23)
- Tyrosinemias (13)
- Urea Cycle Disorders, Inborn (65)
- Vascular Calcification (76)
- Vitamin A Deficiency (60)
- Vitamin B 12 Deficiency (51)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (767)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (8)
- Wasting Syndrome (355)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (458)
- Werner Syndrome (2)
- Wernicke Encephalopathy (9)
- Whipple Disease (1)
- Wolfram Syndrome (9)
- Wolman Disease (30)
- Xanthomatosis (11)
- Xanthomatosis, Cerebrotendinous (9)
- Xeroderma Pigmentosum (11)
- Zellweger Syndrome (6)
- alpha-Mannosidosis (27)
- beta-Mannosidosis (1)