Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (5)
- Acid-Base Imbalance (190)
- Acidosis (214)
- Acidosis, Lactic (45)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (15)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (108)
- Adrenoleukodystrophy (48)
- Albinism (32)
- Albinism, Ocular (3)
- Albinism, Oculocutaneous (14)
- Alexander Disease (1)
- Alkalosis (22)
- Alkalosis, Respiratory (8)
- Alkaptonuria (7)
- Amino Acid Metabolism, Inborn Errors (254)
- Amyloid Neuropathies (29)
- Amyloid Neuropathies, Familial (27)
- Amyloidosis (582)
- Amyloidosis, Familial (43)
- Amyotrophic Lateral Sclerosis (656)
- Anemia, Iron-Deficiency (552)
- Anemia, Pernicious (2)
- Argininosuccinic Aciduria (5)
- Arthritis, Gouty (25)
- Ascorbic Acid Deficiency (9)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (29)
- Avitaminosis (809)
- Barth Syndrome (6)
- Beriberi (21)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (22)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,465)
- Brain Diseases, Metabolic (895)
- Brain Diseases, Metabolic, Inborn (748)
- CREST Syndrome (7)
- Calcinosis (253)
- Calciphylaxis (12)
- Calcium Metabolism Disorders (426)
- Canavan Disease (7)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (8)
- Carbohydrate Metabolism, Inborn Errors (459)
- Celiac Disease (233)
- Cerebral Amyloid Angiopathy (13)
- Cerebral Amyloid Angiopathy, Familial (13)
- Child Nutrition Disorders (67)
- 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 (69)
- Congenital Disorders of Glycosylation (8)
- Congenital Hyperinsulinism (36)
- Coproporphyria, Hereditary (9)
- Crigler-Najjar Syndrome (12)
- Cystinosis (28)
- Cystinuria (19)
- DNA Repair-Deficiency Disorders (247)
- Deficiency Diseases (1,025)
- Dehydration (146)
- Dent Disease (9)
- Diabetes Mellitus (15,151)
- Diabetes Mellitus, Experimental (2)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,494)
- Diabetes Mellitus, Type 2 (7,340)
- Diabetes, Gestational (476)
- Diabetic Ketoacidosis (40)
- Dyslipidemias (2,338)
- Fabry Disease (157)
- Familial Hypophosphatemic Rickets (42)
- 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 (18)
- Friedreich Ataxia (59)
- Frontotemporal Dementia (175)
- Frontotemporal Lobar Degeneration (165)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (8)
- Gangliosidoses (26)
- Gangliosidoses, GM2 (20)
- Gangliosidosis, GM1 (10)
- Gaucher Disease (110)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (860)
- Glucose Metabolism Disorders (12,913)
- Glucosephosphate Dehydrogenase Deficiency (42)
- Glycogen Storage Disease (140)
- Glycogen Storage Disease Type I (10)
- Glycogen Storage Disease Type II (108)
- Glycogen Storage Disease Type III (6)
- Glycogen Storage Disease Type IIb (2)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (12)
- Glycogen Storage Disease Type VI (2)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (2)
- Gout (225)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (24)
- Hemochromatosis (49)
- Hemosiderosis (27)
- Hepatic Encephalopathy (145)
- Hepatolenticular Degeneration (26)
- Hereditary Central Nervous System Demyelinating Diseases (78)
- Hermanski-Pudlak Syndrome (8)
- Homocystinuria (9)
- Hyperargininemia (4)
- Hypercalcemia (51)
- Hypercholesterolemia (1,037)
- Hyperglycemia (1,077)
- Hyperhomocysteinemia (41)
- Hyperinsulinism (2,444)
- Hyperkalemia (60)
- Hyperlactatemia (23)
- Hyperlipidemia, Familial Combined (37)
- Hyperlipidemias (1,717)
- Hyperlipoproteinemia Type I (21)
- Hyperlipoproteinemia Type II (154)
- Hyperlipoproteinemia Type III (5)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (9)
- Hyperlipoproteinemias (1,685)
- Hypernatremia (30)
- Hyperoxaluria, Primary (34)
- Hyperphosphatemia (140)
- Hypertriglyceridemia (259)
- Hypertriglyceridemic Waist (4)
- Hypervitaminosis A (2)
- Hypoalphalipoproteinemias (14)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (12)
- Hypocalcemia (107)
- Hypoglycemia (635)
- Hypokalemia (32)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (24)
- Hyponatremia (132)
- Hypophosphatasia (29)
- Hypophosphatemia (64)
- Hypophosphatemia, Familial (41)
- Ichthyosis, X-Linked (59)
- Immunoglobulin Light-chain Amyloidosis (155)
- Inappropriate ADH Syndrome (19)
- Infant Nutrition Disorders (32)
- Insulin Resistance (2,775)
- Iron Metabolism Disorders (629)
- Iron Overload (196)
- Kearns-Sayre Syndrome (7)
- Kernicterus (7)
- Ketosis (94)
- Kwashiorkor (23)
- Lactose Intolerance (36)
- 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 (2,825)
- Lipid Metabolism, Inborn Errors (669)
- Lipidoses (402)
- Lipodystrophy (164)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (10)
- Lipomatosis (6)
- Lipomatosis, Multiple Symmetrical (6)
- Lysosomal Storage Diseases (676)
- MELAS Syndrome (14)
- Magnesium Deficiency (19)
- Malabsorption Syndromes (400)
- Malnutrition (2,282)
- Mannosidase Deficiency Diseases (25)
- Maple Syrup Urine Disease (2)
- Menkes Kinky Hair Syndrome (3)
- Metabolic Diseases (21,457)
- Metabolic Syndrome (1,489)
- Metabolism, Inborn Errors (2,010)
- Metal Metabolism, Inborn Errors (159)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (1)
- Mitochondrial Diseases (194)
- Mitochondrial Encephalomyopathies (19)
- Mitochondrial Myopathies (38)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (11)
- Mucopolysaccharidoses (167)
- Mucopolysaccharidosis I (56)
- Mucopolysaccharidosis II (50)
- Mucopolysaccharidosis III (37)
- Mucopolysaccharidosis IV (176)
- 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 (29)
- Niemann-Pick Disease, Type A (48)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (48)
- Niemann-Pick Diseases (48)
- Nutrition Disorders (5,503)
- Obesity (8,421)
- Obesity Hypoventilation Syndrome (44)
- Obesity, Abdominal (184)
- Obesity, Metabolically Benign (9)
- Obesity, Morbid (625)
- Oculocerebrorenal Syndrome (5)
- Ophthalmoplegia, Chronic Progressive External (8)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (30)
- Ornithine Carbamoyltransferase Deficiency Disease (15)
- Osteomalacia (38)
- Osteoporosis (1,330)
- Osteoporosis, Postmenopausal (252)
- Overnutrition (3,315)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (695)
- Pelizaeus-Merzbacher Disease (5)
- Peroxisomal Disorders (54)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (100)
- Phosphorus Metabolism Disorders (178)
- Piebaldism (4)
- Porphyria Cutanea Tarda (38)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (46)
- Porphyria, Variegate (7)
- Porphyrias (46)
- Porphyrias, Hepatic (38)
- Potassium Deficiency (32)
- Prader-Willi Syndrome (91)
- Prediabetic State (660)
- Primary Progressive Nonfluent Aphasia (13)
- Progeria (8)
- Propionic Acidemia (11)
- Protein Deficiency (34)
- Protein-Energy Malnutrition (41)
- Protoporphyria, Erythropoietic (15)
- Pseudohypoaldosteronism (5)
- Pseudohypoparathyroidism (12)
- Pseudopseudohypoparathyroidism (12)
- Purine-Pyrimidine Metabolism, Inborn Errors (139)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (3)
- Pyruvate Metabolism, Inborn Errors (20)
- Refeeding Syndrome (9)
- Refsum Disease (6)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (150)
- Rickets (164)
- Rickets, Hypophosphatemic (42)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (17)
- Scurvy (8)
- Severe Acute Malnutrition (61)
- Severe Combined Immunodeficiency (69)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (144)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (343)
- Sprue, Tropical (8)
- Starvation (16)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (70)
- Sulfatidosis (30)
- Swayback (17)
- TDP-43 Proteinopathies (647)
- Tangier Disease (5)
- Tay-Sachs Disease (22)
- Tetany (324)
- Thiamine Deficiency (21)
- Tyrosinemias (12)
- Urea Cycle Disorders, Inborn (57)
- Vascular Calcification (69)
- Vitamin A Deficiency (54)
- Vitamin B 12 Deficiency (44)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (671)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (6)
- Wasting Syndrome (309)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (386)
- Werner Syndrome (1)
- Wernicke Encephalopathy (8)
- Whipple Disease (1)
- Wolfram Syndrome (8)
- Wolman Disease (28)
- Xanthomatosis (9)
- Xanthomatosis, Cerebrotendinous (7)
- Xeroderma Pigmentosum (10)
- Zellweger Syndrome (5)
- alpha-Mannosidosis (25)
- beta-Mannosidosis (1)