Conditions by Category > Nutritional and Metabolic Diseases
- Abetalipoproteinemia (3)
- Achlorhydria (5)
- Acid-Base Imbalance (213)
- Acidosis (232)
- Acidosis, Lactic (47)
- Acidosis, Renal Tubular (9)
- Acidosis, Respiratory (16)
- Adiposis Dolorosa (5)
- Adrenal Hyperplasia, Congenital (120)
- Adrenoleukodystrophy (53)
- Albinism (35)
- Albinism, Ocular (4)
- Albinism, Oculocutaneous (14)
- Alexander Disease (1)
- Alkalosis (22)
- Alkalosis, Respiratory (8)
- Alkaptonuria (8)
- Amino Acid Metabolism, Inborn Errors (282)
- Amyloid Neuropathies (35)
- Amyloid Neuropathies, Familial (33)
- Amyloidosis (643)
- Amyloidosis, Familial (51)
- Amyotrophic Lateral Sclerosis (733)
- Anemia, Iron-Deficiency (609)
- Anemia, Pernicious (3)
- Argininosuccinic Aciduria (7)
- Arthritis, Gouty (27)
- Ascorbic Acid Deficiency (10)
- Aspartylglucosaminuria (5)
- Ataxia Telangiectasia (33)
- Avitaminosis (881)
- Barth Syndrome (6)
- Beriberi (23)
- Biotinidase Deficiency (4)
- Blind Loop Syndrome (27)
- Bloom Syndrome (1)
- Bone Demineralization, Pathologic (7)
- Bone Diseases, Metabolic (1,558)
- Brain Diseases, Metabolic (980)
- Brain Diseases, Metabolic, Inborn (824)
- CREST Syndrome (8)
- Calcinosis (285)
- Calciphylaxis (14)
- Calcium Metabolism Disorders (476)
- Canavan Disease (7)
- Carbamoyl-Phosphate Synthase I Deficiency Disease (7)
- Carbohydrate Metabolism, Inborn Errors (496)
- Celiac Disease (260)
- Cerebral Amyloid Angiopathy (15)
- Cerebral Amyloid Angiopathy, Familial (15)
- Child Nutrition Disorders (80)
- Cholesterol Ester Storage Disease (28)
- Choline Deficiency (4)
- Chondrodysplasia Punctata, Rhizomelic (3)
- Chronic Kidney Disease-Mineral and Bone Disorder (46)
- Citrullinemia (10)
- Cockayne Syndrome (7)
- Collagenous Sprue (1)
- Colorectal Neoplasms, Hereditary Nonpolyposis (75)
- Congenital Disorders of Glycosylation (8)
- Congenital Hyperinsulinism (42)
- Coproporphyria, Hereditary (9)
- Crigler-Najjar Syndrome (12)
- Cystinosis (29)
- Cystinuria (19)
- DNA Repair-Deficiency Disorders (268)
- Deficiency Diseases (1,120)
- Dehydration (164)
- Dent Disease (10)
- Diabetes Mellitus (16,380)
- Diabetes Mellitus, Experimental (3)
- Diabetes Mellitus, Lipoatrophic (31)
- Diabetes Mellitus, Type 1 (2,713)
- Diabetes Mellitus, Type 2 (7,898)
- Diabetes, Gestational (534)
- Diabetic Ketoacidosis (47)
- Dyslipidemias (2,493)
- Fabry Disease (166)
- Familial Hypophosphatemic Rickets (48)
- Familial Multiple Lipomatosis (1)
- Fanconi Anemia (91)
- Fanconi Syndrome (100)
- Farber Lipogranulomatosis (2)
- Female Athlete Triad Syndrome (7)
- Fetal Nutrition Disorders (2)
- Folic Acid Deficiency (21)
- Friedreich Ataxia (70)
- Frontotemporal Dementia (199)
- Frontotemporal Lobar Degeneration (190)
- Fructose Intolerance (9)
- Fructose Metabolism, Inborn Errors (9)
- Fucosidosis (9)
- Galactosemias (8)
- Gangliosidoses (34)
- Gangliosidoses, GM2 (23)
- Gangliosidosis, GM1 (17)
- Gaucher Disease (123)
- Gilbert Disease (2)
- Gitelman Syndrome (4)
- Glucose Intolerance (969)
- Glucose Metabolism Disorders (14,009)
- Glucosephosphate Dehydrogenase Deficiency (43)
- Glycogen Storage Disease (155)
- Glycogen Storage Disease Type I (11)
- Glycogen Storage Disease Type II (113)
- 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 (241)
- HIV Wasting Syndrome (14)
- HIV-Associated Lipodystrophy Syndrome (25)
- Hemochromatosis (49)
- Hemosiderosis (28)
- Hepatic Encephalopathy (156)
- Hepatolenticular Degeneration (33)
- Hereditary Central Nervous System Demyelinating Diseases (84)
- Hermanski-Pudlak Syndrome (9)
- Homocystinuria (9)
- Hyperargininemia (6)
- Hypercalcemia (54)
- Hypercholesterolemia (1,105)
- Hyperglycemia (1,209)
- Hyperhomocysteinemia (42)
- Hyperinsulinism (2,613)
- Hyperkalemia (69)
- Hyperlactatemia (33)
- Hyperlipidemia, Familial Combined (37)
- Hyperlipidemias (1,830)
- Hyperlipoproteinemia Type I (22)
- Hyperlipoproteinemia Type II (173)
- Hyperlipoproteinemia Type III (6)
- Hyperlipoproteinemia Type IV (7)
- Hyperlipoproteinemia Type V (9)
- Hyperlipoproteinemias (1,795)
- Hypernatremia (35)
- Hyperoxaluria, Primary (37)
- Hyperphosphatemia (149)
- Hypertriglyceridemia (271)
- Hypertriglyceridemic Waist (6)
- Hypervitaminosis A (3)
- Hypoalphalipoproteinemias (14)
- Hypobetalipoproteinemia, Familial, Apolipoprotein B (1)
- Hypobetalipoproteinemias (12)
- Hypocalcemia (126)
- Hypoglycemia (696)
- Hypokalemia (36)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemias (24)
- Hyponatremia (144)
- Hypophosphatasia (29)
- Hypophosphatemia (72)
- Hypophosphatemia, Familial (45)
- Ichthyosis, X-Linked (62)
- Immunoglobulin Light-chain Amyloidosis (166)
- Inappropriate ADH Syndrome (21)
- Infant Nutrition Disorders (39)
- Insulin Resistance (2,971)
- Iron Metabolism Disorders (683)
- Iron Overload (206)
- Kearns-Sayre Syndrome (7)
- Kernicterus (8)
- Ketosis (124)
- Kwashiorkor (26)
- Lactose Intolerance (36)
- Latent Autoimmune Diabetes in Adults (8)
- Lecithin Cholesterol Acyltransferase Deficiency (3)
- Leigh Disease (13)
- Lesch-Nyhan Syndrome (4)
- Leukodystrophy, Globoid Cell (24)
- Leukodystrophy, Metachromatic (38)
- Li-Fraumeni Syndrome (14)
- Liddle Syndrome (1)
- Lipid Metabolism Disorders (3,026)
- Lipid Metabolism, Inborn Errors (729)
- Lipidoses (442)
- Lipodystrophy (168)
- Lipodystrophy, Congenital Generalized (11)
- Lipodystrophy, Familial Partial (10)
- Lipomatosis (8)
- Lipomatosis, Multiple Symmetrical (8)
- Lysosomal Storage Diseases (728)
- MELAS Syndrome (16)
- Magnesium Deficiency (19)
- Malabsorption Syndromes (441)
- Malnutrition (2,482)
- Mannosidase Deficiency Diseases (26)
- Maple Syrup Urine Disease (4)
- Menkes Kinky Hair Syndrome (4)
- Metabolic Diseases (23,328)
- Metabolic Syndrome (1,587)
- Metabolism, Inborn Errors (2,189)
- Metal Metabolism, Inborn Errors (175)
- Mevalonate Kinase Deficiency (4)
- Mineralocorticoid Excess Syndrome, Apparent (1)
- Mitochondrial Diseases (223)
- Mitochondrial Encephalomyopathies (21)
- Mitochondrial Myopathies (45)
- Monckeberg Medial Calcific Sclerosis (2)
- Mucolipidoses (12)
- Mucopolysaccharidoses (183)
- Mucopolysaccharidosis I (61)
- Mucopolysaccharidosis II (60)
- Mucopolysaccharidosis III (38)
- Mucopolysaccharidosis IV (194)
- Mucopolysaccharidosis VI (29)
- Mucopolysaccharidosis VII (13)
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency (4)
- Multiple Sulfatase Deficiency Disease (1)
- Necrobiosis Lipoidica (3)
- Nephrocalcinosis (12)
- Nesidioblastosis (1)
- Neuronal Ceroid-Lipofuscinoses (36)
- 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 (6,075)
- Obesity (9,257)
- Obesity Hypoventilation Syndrome (50)
- Obesity, Abdominal (204)
- Obesity, Metabolically Benign (14)
- Obesity, Morbid (702)
- Oculocerebrorenal Syndrome (5)
- Ophthalmoplegia, Chronic Progressive External (9)
- Optic Atrophy, Autosomal Dominant (5)
- Optic Atrophy, Hereditary, Leber (32)
- Ornithine Carbamoyltransferase Deficiency Disease (22)
- Osteomalacia (40)
- Osteoporosis (1,402)
- Osteoporosis, Postmenopausal (270)
- Overnutrition (3,679)
- Paralysis, Hyperkalemic Periodic (3)
- Pediatric Obesity (783)
- Pelizaeus-Merzbacher Disease (5)
- Peroxisomal Disorders (60)
- Phenylketonuria, Maternal (3)
- Phenylketonurias (117)
- Phosphorus Metabolism Disorders (194)
- 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 (101)
- Prediabetic State (757)
- Primary Progressive Nonfluent Aphasia (14)
- Progeria (9)
- Propionic Acidemia (12)
- Protein Deficiency (42)
- Protein-Energy Malnutrition (43)
- Protoporphyria, Erythropoietic (17)
- Pseudohypoaldosteronism (5)
- Pseudohypoparathyroidism (16)
- Pseudopseudohypoparathyroidism (16)
- Purine-Pyrimidine Metabolism, Inborn Errors (147)
- 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 (159)
- Rickets (175)
- Rickets, Hypophosphatemic (47)
- Rothmund-Thomson Syndrome (2)
- Sandhoff Disease (20)
- Scurvy (9)
- Severe Acute Malnutrition (72)
- Severe Combined Immunodeficiency (75)
- Sialic Acid Storage Disease (1)
- Sjogren-Larsson Syndrome (3)
- Skin Diseases, Metabolic (149)
- Smith-Lemli-Opitz Syndrome (14)
- Sphingolipidoses (374)
- Sprue, Tropical (8)
- Starvation (17)
- Steatitis (2)
- Steatorrhea (16)
- Steroid Metabolism, Inborn Errors (79)
- Sulfatidosis (32)
- Swayback (19)
- TDP-43 Proteinopathies (731)
- Tangier Disease (5)
- Tay-Sachs Disease (25)
- Tay-Sachs Disease, AB Variant (3)
- Tetany (336)
- Thiamine Deficiency (23)
- Tyrosinemias (12)
- Urea Cycle Disorders, Inborn (63)
- Vascular Calcification (72)
- Vitamin A Deficiency (58)
- Vitamin B 12 Deficiency (50)
- Vitamin B 6 Deficiency (4)
- Vitamin D Deficiency (733)
- Vitamin E Deficiency (7)
- Vitamin K Deficiency (7)
- Wasting Syndrome (337)
- Water Intoxication (3)
- Water-Electrolyte Imbalance (437)
- 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 (6)
- alpha-Mannosidosis (26)
- beta-Mannosidosis (1)