Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (4)
- Achlorhydria (6)
- Acid-Base Imbalance (257)
- Acidosis (278)
- Acidosis, Lactic (52)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (17)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (136)
- Adrenoleukodystrophy (61)
- Albinism (35)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (4)
- Alkalosis (24)
- Alkalosis, Respiratory (8)
- Alkaptonuria (9)
- Amino Acid Metabolism, Inborn Errors (313)
- Amyloid Neuropathies (45)
- Amyloid Neuropathies, Familial (39)
- Amyloidosis (743)
- Amyloidosis, Familial (62)
- Amyotrophic Lateral Sclerosis (871)
- Anemia, Iron-Deficiency (697)
- Anemia, Pernicious (5)
- Argininosuccinic Aciduria (8)
- Arthritis, Gouty (35)
- Ascorbic Acid Deficiency (13)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (41)
- Avitaminosis (964)
- Barth Syndrome (8)
- Beriberi (24)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (31)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,699)
- Brain Diseases, Metabolic (1,117)
- Brain Diseases, Metabolic, Inborn (940)
- CREST Syndrome (9)
- Calcinosis (323)
- Calciphylaxis (15)
- Calcium Metabolism Disorders (535)
- Canavan Disease (10)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (8)
- Carbohydrate Metabolism, Inborn Errors (557)
- Celiac Disease (293)
- Cerebral Amyloid Angiopathy (19)
- Cerebral Amyloid Angiopathy, Familial (19)
- Child Nutrition Disorders (99)
- Cholesterol Ester Storage Disease (29)
- Choline Deficiency (5)
- Chondrodysplasia Punctata, Rhizomelic (3)
- Chronic Kidney Disease-Mineral and Bone Disorder (50)
- Citrullinemia (11)
- Cockayne Syndrome (9)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (87)
- Congenital Disorders of Glycosylation (10)
- Congenital Hyperinsulinism (48)
- Coproporphyria, Hereditary (12)
- Crigler-Najjar Syndrome (12)
- Cystinosis (31)
- DNA Repair-Deficiency Disorders (295)
- Deficiency Diseases (1,357)
- Dehydration (181)
- Diabetes Mellitus (18,072)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,998)
- Diabetes Mellitus, Type 2 (8,687)
- Diabetes, Gestational (629)
- Diabetic Ketoacidosis (56)
- Dyslipidemias (2,682)
- Fabry Disease (189)
- Familial Hypophosphatemic Rickets (57)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (96)
- Farber Lipogranulomatosis (2)
- Fetal Nutrition Disorders (4)
- Folic Acid Deficiency (23)
- Friedreich Ataxia (77)
- Frontotemporal Dementia (235)
- Frontotemporal Lobar Degeneration (223)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (10)
- Gangliosidoses (36)
- Gangliosidoses, GM2 (24)
- Gangliosidosis, GM1 (17)
- Gaucher Disease (130)
- Gilbert Disease (2)
- Glucose Intolerance (1,132)
- Glucose Metabolism Disorders (15,439)
- Glucosephosphate Dehydrogenase Deficiency (46)
- Glycogen Storage Disease (181)
- Glycogen Storage Disease Type I (14)
- Glycogen Storage Disease Type II (130)
- Glycogen Storage Disease Type III (9)
- Glycogen Storage Disease Type IIb (2)
- 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 (288)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (26)
- Hemochromatosis (52)
- Hemosiderosis (28)
- Hepatic Encephalopathy (177)
- Hepatolenticular Degeneration (46)
- Hereditary Central Nervous System Demyelinating Diseases (95)
- Hermanski-Pudlak Syndrome (10)
- Homocystinuria (11)
- Hyperargininemia (7)
- Hypercalcemia (59)
- Hypercholesterolemia (1,187)
- Hyperferritinemia (3)
- Hyperglycemia (1,365)
- Hyperhomocysteinemia (44)
- Hyperinsulinism (2,832)
- Hyperkalemia (96)
- Hyperlactatemia (41)
- Hyperlipidemia, Familial Combined (41)
- Hyperlipidemias (1,962)
- Hyperlipoproteinemia Type I (25)
- Hyperlipoproteinemia Type II (196)
- Hyperlipoproteinemia Type III (7)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (12)
- Hyperlipoproteinemias (1,925)
- Hypernatremia (42)
- Hyperoxaluria, Primary (40)
- Hyperphosphatemia (157)
- Hypertriglyceridemia (293)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (15)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (14)
- Hypocalcemia (139)
- Hypoglycemia (763)
- Hypokalemia (42)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (26)
- Hyponatremia (153)
- Hypophosphatasia (33)
- Hypophosphatemia (85)
- Hypophosphatemia, Familial (53)
- Ichthyosis, X-Linked (67)
- Immunoglobulin Light-chain Amyloidosis (182)
- Inappropriate ADH Syndrome (24)
- Infant Nutrition Disorders (43)
- Insulin Resistance (3,206)
- Iron Metabolism Disorders (766)
- Iron Overload (214)
- Kearns-Sayre Syndrome (8)
- Kernicterus (8)
- Ketosis (154)
- Kwashiorkor (33)
- Lactose Intolerance (39)
- Latent Autoimmune Diabetes in Adults (10)
- Lecithin Cholesterol Acyltransferase Deficiency (4)
- Leigh Disease (16)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (26)
- Leukodystrophy, Metachromatic (41)
- Li-Fraumeni Syndrome (17)
- Lipid Metabolism Disorders (3,301)
- Lipid Metabolism, Inborn Errors (814)
- Lipidoses (493)
- Lipodystrophy (180)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (12)
- Lipomatosis (23)
- Lipomatosis, Multiple Symmetrical (23)
- Lysosomal Storage Diseases (800)
- MELAS Syndrome (18)
- Magnesium Deficiency (23)
- Malabsorption Syndromes (500)
- Malnutrition (2,747)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (5)
- Menkes Kinky Hair Syndrome (5)
- Metabolic Diseases (25,847)
- Metabolic Syndrome (1,726)
- Metabolism, Inborn Errors (2,362)
- Metal Metabolism, Inborn Errors (203)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (3)
- Mitochondrial Diseases (256)
- Mitochondrial Encephalomyopathies (25)
- Mitochondrial Myopathies (59)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (12)
- Mucopolysaccharidoses (196)
- Mucopolysaccharidosis I (63)
- Mucopolysaccharidosis II (64)
- Mucopolysaccharidosis III (39)
- Mucopolysaccharidosis IV (212)
- Mucopolysaccharidosis VI (30)
- Mucopolysaccharidosis VII (13)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (4)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (4)
- Nephrocalcinosis (15)
- Nesidioblastosis (1)
- Neuronal Ceroid-Lipofuscinoses (41)
- Niemann-Pick Disease, Type A (53)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (53)
- Niemann-Pick Diseases (53)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (6,821)
- Obesity (10,269)
- Obesity Hypoventilation Syndrome (55)
- Obesity, Abdominal (234)
- Obesity, Maternal (49)
- Obesity, Metabolically Benign (19)
- Obesity, Morbid (781)
- Oculocerebrorenal Syndrome (6)
- Ophthalmoplegia, Chronic Progressive External (11)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (34)
- Ornithine Carbamoyltransferase Deficiency Disease (26)
- Osteomalacia (45)
- Osteoporosis (1,513)
- Osteoporosis, Postmenopausal (300)
- Overnutrition (4,161)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (895)
- Pelizaeus-Merzbacher Disease (6)
- Peroxisomal Disorders (67)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (135)
- Phosphorus Metabolism Disorders (212)
- Piebaldism (4)
- Porphyria Cutanea Tarda (46)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (54)
- Porphyria, Variegate (7)
- Porphyrias (54)
- Porphyrias, Hepatic (46)
- Potassium Deficiency (42)
- Prader-Willi Syndrome (111)
- Prediabetic State (903)
- Primary Progressive Nonfluent Aphasia (16)
- Progeria (9)
- Propionic Acidemia (17)
- Protein Deficiency (49)
- Protein-Energy Malnutrition (50)
- Proteostasis Deficiencies (1,284)
- Protoporphyria, Erythropoietic (20)
- Pseudohypoparathyroidism (17)
- Pseudopseudohypoparathyroidism (17)
- Purine-Pyrimidine Metabolism, Inborn Errors (174)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (5)
- Pyruvate Metabolism, Inborn Errors (31)
- Refeeding Syndrome (12)
- Refsum Disease (8)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (172)
- Rickets (199)
- Rickets, Hypophosphatemic (55)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (21)
- Scurvy (12)
- Severe Acute Malnutrition (87)
- Severe Combined Immunodeficiency (80)
- Shwachman-Diamond Syndrome (16)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (162)
- Smith-Lemli-Opitz Syndrome (15)
- Sphingolipidoses (416)
- Sprue, Tropical (9)
- Starvation (17)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (93)
- Sulfatidosis (33)
- Swayback (28)
- Synucleinopathies (3,243)
- TDP-43 Proteinopathies (861)
- Tangier Disease (5)
- Tay-Sachs Disease (26)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (342)
- Thiamine Deficiency (24)
- Tyrosinemias (14)
- Urea Cycle Disorders, Inborn (69)
- Vascular Calcification (81)
- Vitamin A Deficiency (63)
- Vitamin B 12 Deficiency (56)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (803)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (9)
- Wasting Syndrome (380)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (500)
- Werner Syndrome (2)
- Wernicke Encephalopathy (10)
- Whipple Disease (1)
- Wolfram Syndrome (9)
- Wolman Disease (30)
- Xanthomatosis (11)
- Xanthomatosis, Cerebrotendinous (9)
- Xeroderma Pigmentosum (12)
- Zellweger Syndrome (6)
- alpha-Mannosidosis (26)
- beta-Mannosidosis (1)