Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (5)
- Acid-Base Imbalance (196)
- Acidosis (216)
- Acidosis, Lactic (46)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (15)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (120)
- Adrenoleukodystrophy (52)
- Albinism (34)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (1)
- Alkalosis (22)
- Alkalosis, Respiratory (8)
- Alkaptonuria (8)
- Amino Acid Metabolism, Inborn Errors (276)
- Amyloid Neuropathies (32)
- Amyloid Neuropathies, Familial (30)
- Amyloidosis (618)
- Amyloidosis, Familial (45)
- Amyotrophic Lateral Sclerosis (706)
- Anemia, Iron-Deficiency (584)
- Anemia, Pernicious (3)
- Argininosuccinic Aciduria (5)
- Arthritis, Gouty (26)
- Ascorbic Acid Deficiency (10)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (30)
- Avitaminosis (859)
- Barth Syndrome (6)
- Beriberi (22)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (26)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,527)
- Brain Diseases, Metabolic (951)
- Brain Diseases, Metabolic, Inborn (799)
- CREST Syndrome (7)
- Calcinosis (275)
- Calciphylaxis (12)
- Calcium Metabolism Disorders (459)
- Canavan Disease (7)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (6)
- Carbohydrate Metabolism, Inborn Errors (478)
- Celiac Disease (252)
- Cerebral Amyloid Angiopathy (13)
- Cerebral Amyloid Angiopathy, Familial (13)
- Child Nutrition Disorders (75)
- Cholesterol Ester Storage Disease (28)
- Choline Deficiency (4)
- Chondrodysplasia Punctata, Rhizomelic (2)
- Chronic Kidney Disease-Mineral and Bone Disorder (43)
- Citrullinemia (8)
- Cockayne Syndrome (7)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (74)
- Congenital Disorders of Glycosylation (8)
- Congenital Hyperinsulinism (40)
- Coproporphyria, Hereditary (9)
- Crigler-Najjar Syndrome (12)
- Cystinosis (29)
- Cystinuria (19)
- DNA Repair-Deficiency Disorders (265)
- Deficiency Diseases (1,086)
- Dehydration (157)
- Dent Disease (10)
- Diabetes Mellitus (15,960)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,635)
- Diabetes Mellitus, Type 2 (7,700)
- Diabetes, Gestational (516)
- Diabetic Ketoacidosis (45)
- Dyslipidemias (2,430)
- Fabry Disease (162)
- Familial Hypophosphatemic Rickets (47)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (90)
- Fanconi Syndrome (99)
- Farber Lipogranulomatosis (2)
- Female Athlete Triad Syndrome (7)
- Fetal Nutrition Disorders (1)
- Folic Acid Deficiency (19)
- Friedreich Ataxia (66)
- Frontotemporal Dementia (190)
- Frontotemporal Lobar Degeneration (180)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (8)
- Gangliosidoses (31)
- Gangliosidoses, GM2 (21)
- Gangliosidosis, GM1 (15)
- Gaucher Disease (120)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (936)
- Glucose Metabolism Disorders (13,601)
- Glucosephosphate Dehydrogenase Deficiency (42)
- Glycogen Storage Disease (149)
- Glycogen Storage Disease Type I (10)
- Glycogen Storage Disease Type II (111)
- Glycogen Storage Disease Type III (6)
- Glycogen Storage Disease Type IIb (2)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (14)
- Glycogen Storage Disease Type VI (2)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (2)
- Gout (237)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (25)
- Hemochromatosis (49)
- Hemosiderosis (28)
- Hepatic Encephalopathy (152)
- Hepatolenticular Degeneration (32)
- Hereditary Central Nervous System Demyelinating Diseases (81)
- Hermanski-Pudlak Syndrome (9)
- Homocystinuria (9)
- Hyperargininemia (4)
- Hypercalcemia (54)
- Hypercholesterolemia (1,082)
- Hyperglycemia (1,171)
- Hyperhomocysteinemia (42)
- Hyperinsulinism (2,551)
- Hyperkalemia (66)
- Hyperlactatemia (30)
- Hyperlipidemia, Familial Combined (37)
- Hyperlipidemias (1,788)
- Hyperlipoproteinemia Type I (21)
- Hyperlipoproteinemia Type II (168)
- Hyperlipoproteinemia Type III (5)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (9)
- Hyperlipoproteinemias (1,754)
- Hypernatremia (33)
- Hyperoxaluria, Primary (35)
- Hyperphosphatemia (147)
- Hypertriglyceridemia (265)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (14)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (12)
- Hypocalcemia (122)
- Hypoglycemia (675)
- Hypokalemia (36)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (24)
- Hyponatremia (141)
- Hypophosphatasia (29)
- Hypophosphatemia (71)
- Hypophosphatemia, Familial (44)
- Ichthyosis, X-Linked (61)
- Immunoglobulin Light-chain Amyloidosis (162)
- Inappropriate ADH Syndrome (20)
- Infant Nutrition Disorders (37)
- Insulin Resistance (2,906)
- Iron Metabolism Disorders (663)
- Iron Overload (204)
- Kearns-Sayre Syndrome (7)
- Kernicterus (7)
- Ketosis (109)
- Kwashiorkor (23)
- Lactose Intolerance (36)
- Latent Autoimmune Diabetes in Adults (8)
- Lecithin Cholesterol Acyltransferase Deficiency (3)
- Leigh Disease (12)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (23)
- Leukodystrophy, Metachromatic (37)
- Li-Fraumeni Syndrome (14)
- Liddle Syndrome (1)
- Lipid Metabolism Disorders (2,943)
- Lipid Metabolism, Inborn Errors (707)
- Lipidoses (427)
- Lipodystrophy (165)
- Lipodystrophy, Congenital Generalized (10)
- Lipodystrophy, Familial Partial (10)
- Lipomatosis (7)
- Lipomatosis, Multiple Symmetrical (7)
- Lysosomal Storage Diseases (706)
- MELAS Syndrome (15)
- Magnesium Deficiency (19)
- Malabsorption Syndromes (429)
- Malnutrition (2,404)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (3)
- Menkes Kinky Hair Syndrome (4)
- Metabolic Diseases (22,638)
- Metabolic Syndrome (1,555)
- Metabolism, Inborn Errors (2,124)
- Metal Metabolism, Inborn Errors (171)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (1)
- Mitochondrial Diseases (209)
- Mitochondrial Encephalomyopathies (20)
- Mitochondrial Myopathies (41)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (11)
- Mucopolysaccharidoses (175)
- Mucopolysaccharidosis I (60)
- Mucopolysaccharidosis II (55)
- Mucopolysaccharidosis III (37)
- Mucopolysaccharidosis IV (185)
- Mucopolysaccharidosis VI (29)
- Mucopolysaccharidosis VII (13)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (3)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (3)
- Nephrocalcinosis (12)
- Nesidioblastosis (1)
- Neuronal Ceroid-Lipofuscinoses (33)
- Niemann-Pick Disease, Type A (49)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (49)
- Niemann-Pick Diseases (49)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (5,851)
- Obesity (8,950)
- Obesity Hypoventilation Syndrome (47)
- Obesity, Abdominal (197)
- Obesity, Metabolically Benign (12)
- Obesity, Morbid (670)
- Oculocerebrorenal Syndrome (5)
- Ophthalmoplegia, Chronic Progressive External (7)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (31)
- Ornithine Carbamoyltransferase Deficiency Disease (19)
- Osteomalacia (39)
- Osteoporosis (1,378)
- Osteoporosis, Postmenopausal (263)
- Overnutrition (3,534)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (754)
- Pelizaeus-Merzbacher Disease (5)
- Peroxisomal Disorders (57)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (116)
- Phosphorus Metabolism Disorders (192)
- Piebaldism (4)
- Porphyria Cutanea Tarda (39)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (47)
- Porphyria, Variegate (7)
- Porphyrias (47)
- Porphyrias, Hepatic (39)
- Potassium Deficiency (36)
- Prader-Willi Syndrome (97)
- Prediabetic State (726)
- Primary Progressive Nonfluent Aphasia (14)
- Progeria (9)
- Propionic Acidemia (12)
- Protein Deficiency (36)
- Protein-Energy Malnutrition (42)
- Protoporphyria, Erythropoietic (16)
- Pseudohypoaldosteronism (5)
- Pseudohypoparathyroidism (14)
- Pseudopseudohypoparathyroidism (14)
- Purine-Pyrimidine Metabolism, Inborn Errors (143)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (3)
- Pyruvate Metabolism, Inborn Errors (21)
- Refeeding Syndrome (9)
- Refsum Disease (8)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (157)
- Rickets (170)
- Rickets, Hypophosphatemic (46)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (18)
- Scurvy (9)
- Severe Acute Malnutrition (65)
- Severe Combined Immunodeficiency (75)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (146)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (362)
- Sprue, Tropical (8)
- Starvation (17)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (79)
- Sulfatidosis (31)
- Swayback (19)
- TDP-43 Proteinopathies (704)
- Tangier Disease (5)
- Tay-Sachs Disease (23)
- Tay-Sachs Disease, AB Variant (2)
- Tetany (332)
- Thiamine Deficiency (22)
- Tyrosinemias (12)
- Urea Cycle Disorders, Inborn (60)
- Vascular Calcification (71)
- Vitamin A Deficiency (56)
- Vitamin B 12 Deficiency (47)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (714)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (7)
- Wasting Syndrome (321)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (422)
- Werner Syndrome (2)
- Wernicke Encephalopathy (9)
- Whipple Disease (1)
- Wolfram Syndrome (8)
- Wolman Disease (29)
- Xanthomatosis (10)
- Xanthomatosis, Cerebrotendinous (8)
- Xeroderma Pigmentosum (11)
- Zellweger Syndrome (5)
- alpha-Mannosidosis (26)
- beta-Mannosidosis (1)