Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (5)
- Acid-Base Imbalance (223)
- Acidosis (241)
- Acidosis, Lactic (49)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (17)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (124)
- Adrenoleukodystrophy (53)
- Albinism (35)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (1)
- Alkalosis (23)
- Alkalosis, Respiratory (8)
- Alkaptonuria (9)
- Amino Acid Metabolism, Inborn Errors (286)
- Amyloid Neuropathies (36)
- Amyloid Neuropathies, Familial (33)
- Amyloidosis (659)
- Amyloidosis, Familial (53)
- Amyotrophic Lateral Sclerosis (754)
- Anemia, Iron-Deficiency (628)
- Anemia, Pernicious (3)
- Argininosuccinic Aciduria (7)
- Arthritis, Gouty (28)
- Ascorbic Acid Deficiency (10)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (34)
- Avitaminosis (898)
- Barth Syndrome (6)
- Beriberi (23)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (29)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,587)
- Brain Diseases, Metabolic (1,004)
- Brain Diseases, Metabolic, Inborn (842)
- CREST Syndrome (8)
- Calcinosis (291)
- Calciphylaxis (14)
- Calcium Metabolism Disorders (492)
- Canavan Disease (8)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (7)
- Carbohydrate Metabolism, Inborn Errors (503)
- Celiac Disease (269)
- Cerebral Amyloid Angiopathy (17)
- Cerebral Amyloid Angiopathy, Familial (17)
- Child Nutrition Disorders (84)
- Cholesterol Ester Storage Disease (29)
- Choline Deficiency (4)
- Chondrodysplasia Punctata, Rhizomelic (3)
- Chronic Kidney Disease-Mineral and Bone Disorder (47)
- Citrullinemia (10)
- Cockayne Syndrome (7)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (78)
- Congenital Disorders of Glycosylation (9)
- Congenital Hyperinsulinism (46)
- Coproporphyria, Hereditary (9)
- Crigler-Najjar Syndrome (12)
- Cystinosis (29)
- Cystinuria (20)
- DNA Repair-Deficiency Disorders (273)
- Deficiency Diseases (1,140)
- Dehydration (167)
- Dent Disease (10)
- Diabetes Mellitus (16,679)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,768)
- Diabetes Mellitus, Type 2 (8,026)
- Diabetes, Gestational (544)
- Diabetic Ketoacidosis (49)
- Dyslipidemias (2,520)
- Fabry Disease (171)
- Familial Hypophosphatemic Rickets (51)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (93)
- Fanconi Syndrome (102)
- Farber Lipogranulomatosis (2)
- Female Athlete Triad Syndrome (9)
- Fetal Nutrition Disorders (3)
- Folic Acid Deficiency (21)
- Friedreich Ataxia (72)
- Frontotemporal Dementia (203)
- Frontotemporal Lobar Degeneration (194)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (8)
- Gangliosidoses (35)
- Gangliosidoses, GM2 (24)
- Gangliosidosis, GM1 (17)
- Gaucher Disease (126)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (998)
- Glucose Metabolism Disorders (14,277)
- Glucosephosphate Dehydrogenase Deficiency (43)
- Glycogen Storage Disease (159)
- Glycogen Storage Disease Type I (11)
- Glycogen Storage Disease Type II (117)
- Glycogen Storage Disease Type III (7)
- Glycogen Storage Disease Type IIb (2)
- Glycogen Storage Disease Type IV (4)
- Glycogen Storage Disease Type V (15)
- Glycogen Storage Disease Type VI (2)
- Glycogen Storage Disease Type VII (4)
- Glycogen Storage Disease Type VIII (1)
- Glycosuria, Renal (2)
- Gout (254)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (25)
- Hemochromatosis (50)
- Hemosiderosis (28)
- Hepatic Encephalopathy (161)
- Hepatolenticular Degeneration (33)
- Hereditary Central Nervous System Demyelinating Diseases (86)
- Hermanski-Pudlak Syndrome (9)
- Homocystinuria (9)
- Hyperargininemia (6)
- Hypercalcemia (54)
- Hypercholesterolemia (1,121)
- Hyperglycemia (1,232)
- Hyperhomocysteinemia (42)
- Hyperinsulinism (2,660)
- Hyperkalemia (75)
- Hyperlactatemia (35)
- Hyperlipidemia, Familial Combined (38)
- Hyperlipidemias (1,850)
- Hyperlipoproteinemia Type I (22)
- Hyperlipoproteinemia Type II (179)
- Hyperlipoproteinemia Type III (6)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (9)
- Hyperlipoproteinemias (1,814)
- Hypernatremia (36)
- Hyperoxaluria, Primary (37)
- Hyperphosphatemia (154)
- Hypertriglyceridemia (273)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (15)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (12)
- Hypocalcemia (130)
- Hypoglycemia (710)
- Hypokalemia (36)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (25)
- Hyponatremia (147)
- Hypophosphatasia (29)
- Hypophosphatemia (76)
- Hypophosphatemia, Familial (48)
- Ichthyosis, X-Linked (62)
- Immunoglobulin Light-chain Amyloidosis (168)
- Inappropriate ADH Syndrome (22)
- Infant Nutrition Disorders (39)
- Insulin Resistance (3,018)
- Iron Metabolism Disorders (702)
- Iron Overload (209)
- Kearns-Sayre Syndrome (7)
- Kernicterus (8)
- Ketosis (131)
- Kwashiorkor (27)
- Lactose Intolerance (37)
- Latent Autoimmune Diabetes in Adults (8)
- Lecithin Cholesterol Acyltransferase Deficiency (4)
- Leigh Disease (13)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (25)
- Leukodystrophy, Metachromatic (38)
- Li-Fraumeni Syndrome (14)
- Liddle Syndrome (1)
- Lipid Metabolism Disorders (3,068)
- Lipid Metabolism, Inborn Errors (749)
- Lipidoses (455)
- Lipodystrophy (168)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (10)
- Lipomatosis (9)
- Lipomatosis, Multiple Symmetrical (9)
- Lysosomal Storage Diseases (742)
- MELAS Syndrome (16)
- Magnesium Deficiency (19)
- Malabsorption Syndromes (454)
- Malnutrition (2,534)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (5)
- Menkes Kinky Hair Syndrome (4)
- Metabolic Diseases (23,805)
- Metabolic Syndrome (1,617)
- Metabolism, Inborn Errors (2,237)
- Metal Metabolism, Inborn Errors (179)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (1)
- Mitochondrial Diseases (230)
- Mitochondrial Encephalomyopathies (22)
- Mitochondrial Myopathies (47)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (12)
- Mucopolysaccharidoses (184)
- Mucopolysaccharidosis I (61)
- Mucopolysaccharidosis II (60)
- Mucopolysaccharidosis III (38)
- Mucopolysaccharidosis IV (195)
- Mucopolysaccharidosis VI (29)
- Mucopolysaccharidosis VII (13)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (4)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (4)
- Nephrocalcinosis (12)
- Nesidioblastosis (1)
- Neuronal Ceroid-Lipofuscinoses (38)
- Niemann-Pick Disease, Type A (48)
- Niemann-Pick Disease, Type B (1)
- Niemann-Pick Disease, Type C (48)
- Niemann-Pick Diseases (48)
- Nijmegen Breakage Syndrome (1)
- Nutrition Disorders (6,217)
- Obesity (9,456)
- Obesity Hypoventilation Syndrome (52)
- Obesity, Abdominal (212)
- Obesity, Metabolically Benign (14)
- Obesity, Morbid (721)
- Oculocerebrorenal Syndrome (5)
- Ophthalmoplegia, Chronic Progressive External (9)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (32)
- Ornithine Carbamoyltransferase Deficiency Disease (22)
- Osteomalacia (44)
- Osteoporosis (1,423)
- Osteoporosis, Postmenopausal (276)
- Overnutrition (3,770)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (807)
- Pelizaeus-Merzbacher Disease (5)
- Peroxisomal Disorders (60)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (118)
- Phosphorus Metabolism Disorders (203)
- Piebaldism (4)
- Porphyria Cutanea Tarda (40)
- Porphyria, Acute Intermittent (19)
- Porphyria, Erythropoietic (48)
- Porphyria, Variegate (7)
- Porphyrias (48)
- Porphyrias, Hepatic (40)
- Potassium Deficiency (36)
- Prader-Willi Syndrome (102)
- Prediabetic State (780)
- Primary Progressive Nonfluent Aphasia (14)
- Progeria (9)
- Propionic Acidemia (13)
- Protein Deficiency (43)
- Protein-Energy Malnutrition (44)
- Proteostasis Deficiencies (1,104)
- Protoporphyria, Erythropoietic (17)
- Pseudohypoaldosteronism (5)
- Pseudohypoparathyroidism (16)
- Pseudopseudohypoparathyroidism (16)
- Purine-Pyrimidine Metabolism, Inborn Errors (154)
- Pyruvate Carboxylase Deficiency Disease (1)
- Pyruvate Dehydrogenase Complex Deficiency Disease (4)
- Pyruvate Metabolism, Inborn Errors (23)
- Refeeding Syndrome (9)
- Refsum Disease (8)
- Refsum Disease, Infantile (4)
- Renal Tubular Transport, Inborn Errors (164)
- Rickets (184)
- Rickets, Hypophosphatemic (50)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (21)
- Scurvy (9)
- Severe Acute Malnutrition (74)
- Severe Combined Immunodeficiency (76)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (150)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (383)
- Sprue, Tropical (8)
- Starvation (17)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (81)
- Sulfatidosis (32)
- Swayback (19)
- TDP-43 Proteinopathies (751)
- Tangier Disease (5)
- Tay-Sachs Disease (26)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (337)
- Thiamine Deficiency (23)
- Tyrosinemias (13)
- Urea Cycle Disorders, Inborn (63)
- Vascular Calcification (74)
- Vitamin A Deficiency (60)
- Vitamin B 12 Deficiency (51)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (749)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (7)
- Wasting Syndrome (343)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (450)
- Werner Syndrome (2)
- Wernicke Encephalopathy (9)
- Whipple Disease (1)
- Wolfram Syndrome (8)
- Wolman Disease (30)
- Xanthomatosis (10)
- Xanthomatosis, Cerebrotendinous (8)
- Xeroderma Pigmentosum (11)
- Zellweger Syndrome (6)
- alpha-Mannosidosis (26)
- beta-Mannosidosis (1)