Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (4)
- Acid-Base Imbalance (181)
- Acidosis (205)
- Acidosis, Lactic (45)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (14)
- Adiposis Dolorosa (4)
- Adrenal Hyperplasia, Congenital (107)
- Adrenoleukodystrophy (48)
- Albinism (31)
- Albinism, Ocular (3)
- Albinism, Oculocutaneous (13)
- Alexander Disease (1)
- Alkalosis (21)
- Alkalosis, Respiratory (7)
- Alkaptonuria (5)
- Amino Acid Metabolism, Inborn Errors (244)
- Amyloid Neuropathies (26)
- Amyloid Neuropathies, Familial (25)
- Amyloidosis (564)
- Amyloidosis, Familial (40)
- Amyotrophic Lateral Sclerosis (637)
- Anemia, Iron-Deficiency (531)
- Anemia, Pernicious (2)
- Argininosuccinic Aciduria (5)
- Arthritis, Gouty (20)
- Ascorbic Acid Deficiency (9)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (28)
- Avitaminosis (786)
- Barth Syndrome (6)
- Beriberi (21)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (21)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,442)
- Brain Diseases, Metabolic (862)
- Brain Diseases, Metabolic, Inborn (722)
- CREST Syndrome (7)
- Calcinosis (247)
- Calciphylaxis (11)
- Calcium Metabolism Disorders (409)
- Canavan Disease (6)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (8)
- Carbohydrate Metabolism, Inborn Errors (439)
- Celiac Disease (225)
- Cerebral Amyloid Angiopathy (12)
- Cerebral Amyloid Angiopathy, Familial (12)
- Child Nutrition Disorders (62)
- Cholesterol Ester Storage Disease (27)
- Choline Deficiency (4)
- Chondrodysplasia Punctata, Rhizomelic (2)
- Chronic Kidney Disease-Mineral and Bone Disorder (40)
- Citrullinemia (8)
- Cockayne Syndrome (7)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (64)
- Congenital Disorders of Glycosylation (5)
- Congenital Hyperinsulinism (34)
- Coproporphyria, Hereditary (9)
- Crigler-Najjar Syndrome (11)
- Cystinosis (27)
- Cystinuria (17)
- DNA Repair-Deficiency Disorders (240)
- Deficiency Diseases (992)
- Dehydration (145)
- Dent Disease (9)
- Diabetes Mellitus (14,761)
- Diabetes Mellitus, Experimental (2)
- Diabetes Mellitus, Lipoatrophic (30)
- Diabetes Mellitus, Type 1 (2,414)
- Diabetes Mellitus, Type 2 (7,153)
- Diabetes, Gestational (454)
- Diabetic Ketoacidosis (38)
- Dyslipidemias (2,292)
- Fabry Disease (154)
- Familial Hypophosphatemic Rickets (38)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (85)
- Fanconi Syndrome (94)
- Farber Lipogranulomatosis (2)
- Female Athlete Triad Syndrome (7)
- Fetal Nutrition Disorders (1)
- Folic Acid Deficiency (15)
- Friedreich Ataxia (56)
- Frontotemporal Dementia (163)
- Frontotemporal Lobar Degeneration (154)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (7)
- Gangliosidoses (25)
- Gangliosidoses, GM2 (19)
- Gangliosidosis, GM1 (10)
- Gaucher Disease (105)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (839)
- Glucose Metabolism Disorders (12,565)
- Glucosephosphate Dehydrogenase Deficiency (40)
- Glycogen Storage Disease (133)
- Glycogen Storage Disease Type I (9)
- Glycogen Storage Disease Type II (103)
- Glycogen Storage Disease Type III (6)
- Glycogen Storage Disease Type IIb (2)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (11)
- Glycogen Storage Disease Type VI (2)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (2)
- Gout (218)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (24)
- Hemochromatosis (48)
- Hemosiderosis (27)
- Hepatic Encephalopathy (139)
- Hepatolenticular Degeneration (25)
- Hereditary Central Nervous System Demyelinating Diseases (77)
- Hermanski-Pudlak Syndrome (7)
- Homocystinuria (9)
- Hyperargininemia (4)
- Hypercalcemia (52)
- Hypercholesterolemia (1,019)
- Hyperglycemia (1,051)
- Hyperhomocysteinemia (41)
- Hyperinsulinism (2,376)
- Hyperkalemia (57)
- Hyperlactatemia (21)
- Hyperlipidemia, Familial Combined (37)
- Hyperlipidemias (1,686)
- Hyperlipoproteinemia Type I (19)
- Hyperlipoproteinemia Type II (149)
- Hyperlipoproteinemia Type III (5)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (9)
- Hyperlipoproteinemias (1,655)
- Hypernatremia (29)
- Hyperoxaluria, Primary (32)
- Hyperphosphatemia (140)
- Hypertriglyceridemia (253)
- Hypertriglyceridemic Waist (4)
- Hypervitaminosis A (2)
- Hypoalphalipoproteinemias (14)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (9)
- Hypocalcemia (96)
- Hypoglycemia (614)
- Hypokalemia (31)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (24)
- Hyponatremia (130)
- Hypophosphatasia (25)
- Hypophosphatemia (60)
- Hypophosphatemia, Familial (38)
- Ichthyosis, X-Linked (56)
- Immunoglobulin Light-chain Amyloidosis (153)
- Inappropriate ADH Syndrome (18)
- Infant Nutrition Disorders (31)
- Insulin Resistance (2,705)
- Iron Metabolism Disorders (613)
- Iron Overload (193)
- Kearns-Sayre Syndrome (7)
- Kernicterus (7)
- Ketosis (86)
- Kwashiorkor (23)
- Lactose Intolerance (35)
- Latent Autoimmune Diabetes in Adults (7)
- Lecithin Cholesterol Acyltransferase Deficiency (3)
- Leigh Disease (11)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (23)
- Leukodystrophy, Metachromatic (35)
- Li-Fraumeni Syndrome (13)
- Liddle Syndrome (1)
- Lipid Metabolism Disorders (2,760)
- Lipid Metabolism, Inborn Errors (647)
- Lipidoses (391)
- Lipodystrophy (162)
- Lipodystrophy, Congenital Generalized (9)
- Lipodystrophy, Familial Partial (10)
- Lipomatosis (5)
- Lipomatosis, Multiple Symmetrical (1)
- Lysosomal Storage Diseases (657)
- MELAS Syndrome (13)
- Magnesium Deficiency (16)
- Malabsorption Syndromes (389)
- Malnutrition (2,211)
- Mannosidase Deficiency Diseases (25)
- Maple Syrup Urine Disease (2)
- Menkes Kinky Hair Syndrome (3)
- Metabolic Diseases (20,863)
- Metabolic Syndrome (1,454)
- Metabolism, Inborn Errors (1,932)
- Metal Metabolism, Inborn Errors (150)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (1)
- Mitochondrial Diseases (187)
- Mitochondrial Encephalomyopathies (17)
- Mitochondrial Myopathies (36)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (11)
- Mucopolysaccharidoses (164)
- Mucopolysaccharidosis I (55)
- Mucopolysaccharidosis II (50)
- Mucopolysaccharidosis III (36)
- Mucopolysaccharidosis IV (166)
- 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 (28)
- Niemann-Pick Disease, Type A (46)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (46)
- Niemann-Pick Diseases (46)
- Nutrition Disorders (5,284)
- Obesity (8,127)
- Obesity Hypoventilation Syndrome (41)
- Obesity, Abdominal (174)
- Obesity, Metabolically Benign (9)
- Obesity, Morbid (595)
- Oculocerebrorenal Syndrome (5)
- Ophthalmoplegia, Chronic Progressive External (8)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (30)
- Ornithine Carbamoyltransferase Deficiency Disease (15)
- Osteomalacia (37)
- Osteoporosis (1,311)
- Osteoporosis, Postmenopausal (245)
- Overnutrition (3,177)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (660)
- Pelizaeus-Merzbacher Disease (5)
- Peroxisomal Disorders (54)
- Phenylketonurias (96)
- Phosphorus Metabolism Disorders (174)
- Piebaldism (4)
- Porphyria Cutanea Tarda (38)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (46)
- Porphyria, Variegate (7)
- Porphyrias (46)
- Porphyrias, Hepatic (38)
- Potassium Deficiency (31)
- Prader-Willi Syndrome (87)
- Prediabetic State (639)
- Primary Progressive Nonfluent Aphasia (13)
- Progeria (8)
- Propionic Acidemia (9)
- Protein Deficiency (32)
- Protein-Energy Malnutrition (40)
- Protoporphyria, Erythropoietic (15)
- Pseudohypoaldosteronism (4)
- Pseudohypoparathyroidism (12)
- Pseudopseudohypoparathyroidism (12)
- Purine-Pyrimidine Metabolism, Inborn Errors (134)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (3)
- Pyruvate Metabolism, Inborn Errors (19)
- Refeeding Syndrome (9)
- Refsum Disease (6)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (145)
- Rickets (160)
- Rickets, Hypophosphatemic (38)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (16)
- Scurvy (8)
- Severe Acute Malnutrition (60)
- Severe Combined Immunodeficiency (67)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (142)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (333)
- Sprue, Tropical (8)
- Starvation (16)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (69)
- Sulfatidosis (30)
- Swayback (16)
- TDP-43 Proteinopathies (628)
- Tangier Disease (5)
- Tay-Sachs Disease (21)
- Tetany (318)
- Thiamine Deficiency (21)
- Tyrosinemias (10)
- Urea Cycle Disorders, Inborn (57)
- Vascular Calcification (67)
- Vitamin A Deficiency (49)
- Vitamin B 12 Deficiency (44)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (655)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (5)
- Wasting Syndrome (299)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (377)
- Werner Syndrome (1)
- Wernicke Encephalopathy (8)
- Whipple Disease (1)
- Wolfram Syndrome (8)
- Wolman Disease (28)
- Xanthomatosis (7)
- Xanthomatosis, Cerebrotendinous (5)
- Xeroderma Pigmentosum (9)
- Zellweger Syndrome (5)
- alpha-Mannosidosis (25)
- beta-Mannosidosis (1)