NIH/National Institute of Diabetes, Digestive & Kidney Diseases
Office of Communications & Public Liaison
Bethesda, MD
3014963583
About NIH/National Institute of Diabetes, Digestive & Kidney Diseases
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) conducts and supports research on many of the most serious diseases affecting public health. The Institute supports much of the clinical research on the diseases of internal medicine and related subspecialty fields, as well as many basic science disciplines. The Institute’s Division of Intramural Research encompasses the broad spectrum of metabolic diseases such as diabetes, obesity, inborn errors of metabolism, endocrine disorders, mineral metabolism, digestive and liver diseases, nutrition, urology and renal disease, and hematology. Basic research studies include biochemistry, biophysics, nutrition, pathology, histochemistry, bioorganic chemistry, physical chemistry, chemical and molecular biology, and pharmacology.
Related Rare Diseases:
- Liddle Syndrome
- Hepatitis D
- Pediatric Crohn’s Disease
- Primary Distal Renal Tubular Acidosis
- Superior Mesenteric Artery Syndrome
- Primary Hyperparathyroidism
- Autoimmune Hepatitis
- Gitelman Syndrome
- Dent Disease
- Familial Partial Lipodystrophy
- Congenital Generalized Lipodystrophy
- Ogilvie syndrome
- Low Gamma-GT Familial Intrahepatic Cholestasis
- Hepatic Encephalopathy
- Multiple Endocrine Neoplasia Type 2
- Ferroportin Disease
- Juvenile Hemochromatosis
- Multiple Endocrine Neoplasia Type 1
- Gastroparesis
- Arginine Vasopressin Deficiency
- Refractory Celiac Disease
- Menetrier Disease
- Lysosomal Storage Disorders
- Rabson-Mendenhall Syndrome
- Turcot Syndrome
- Cytochrome C Oxidase Deficiency
- Cat Eye Syndrome
- Short Chain Acyl CoA Dehydrogenase Deficiency
- Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)
- Duodenal Atresia or Stenosis
- Degos Disease
- Esophageal Atresia and/or Tracheoesophageal Fistula
- Gastroschisis
- Aspartylglycosaminuria
- Carnitine Palmitoyltransferase 1A Deficiency
- Phosphoglycerate Kinase Deficiency
- Cyclic Vomiting Syndrome
- Jejunal Atresia
- Vitamin D Deficiency Rickets
- PEPCK Deficiency
- Pyruvate Carboxylase Deficiency
- Autoimmune Polyendocrine Syndrome Type II
- Wolfram Syndrome
- Retroperitoneal Fibrosis
- Proctitis
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Keratomalacia
- Hyperkalemia
- Glucose-Galactose Malabsorption
- Hypokalemia
- STEC Hemolytic Uremic Syndrome
- Mallory Weiss Syndrome
- Eosinophilic Gastroenteritis
- Dubin Johnson Syndrome
- Hirschsprung Disease
- Banti’s Syndrome
- Pancreatic Neuroendocrine Neoplasms (pNENs)
- Microvillus Inclusion Disease
- Acute Cholecystitis
- Mucopolysaccharidoses
- Renal Glycosuria
- Porphyrias
- Polycystic Liver Disease
- Imperforate Anus
- Valinemia
- Pseudohypoparathyroidism
- Histidinemia
- Caroli Disease
- Primary Biliary Cholangitis
- Bartter Syndrome
- Budd Chiari Syndrome
- Hyperprolinemia Type I
- Hyperprolinemia Type II
- Acrodermatitis Enteropathica
- Dercum’s Disease
- Prune Belly Syndrome
- Familial Lipoprotein Lipase Deficiency
- Alagille Syndrome
- Primary Hyperoxaluria
- Acquired Lipodystrophy
- Mesenteric Panniculitis
- Chronic Intestinal Pseudo-Obstruction
- Alpha-Mannosidosis
- Primary Sclerosing Cholangitis
- Familial Hypophosphatemia
- Glycogen Storage Disease Type VI
- Glycogen Storage Disease Type IX
- Glycogen Storage Disease Type 7
- Glycogen Storage Disease Type V
- Andersen Disease (GSD IV)
- Glycogen Storage Disease Type I
- Galactosemia
- Shwachman Diamond Syndrome
- Zollinger-Ellison Syndrome
- Nephrogenic Diabetes Insipidus
- Variegate Porphyria
- Erythropoietic Protoporphyria and X-Linked Protoporphyria
- Porphyria Cutanea Tarda
- ALAD Porphyria
- Congenital Erythropoietic Porphyria
- Gilbert Syndrome
- N-Acetylglutamate Synthetase Deficiency
- Arginase-1 Deficiency
- Ornithine Transcarbamylase Deficiency
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Mucolipidosis IV
- I Cell Disease
- Pseudo Hurler Polydystrophy
- Sialidosis
- Mucopolysaccharidosis IV
- Mucopolysaccharidosis Type III
- Maroteaux Lamy Syndrome
- Mucopolysaccharidosis Type II
- Kernicterus
- Sheehan Syndrome
- Celiac Disease
- Neonatal Cholestasis
- Biliary Atresia
- Barrett Esophagus
- Wernicke-Korsakoff Syndrome
- Blue Diaper Syndrome
- Peutz Jeghers Syndrome
- Achard Thiers Syndrome
- Primary Intestinal Lymphangiectasia
- Whipple Disease
- Tropical Sprue
- Ulcerative Colitis
- Acromegaly
- Addison’s Disease
- Cystic Fibrosis
- Classic Hereditary Hemochromatosis
- Fibrosis quística
- Síndrome del ojo de gato
- Síndrome de Sheehan
- Paniculitis Mesentérica
- Pseudohipoparatiroidismo
- Deficiencia de Arginasa-1
- Enfermedad de Degos
- Mucopolisacaridosis IV
- Gastrosquisis
- Diabetes insípida nefrogénica
- Hiperparatiroidismo primario
- Porfirias
- Acromegalia
- Lipodistrofia generalizada congénita
- Glucosuria renal
- Enfermedad poliquística del hígado
- Hepatitis D
- Hiperprolinemia tipo I
- Raquitismo por deficiencia de vitamina D
- Hiperoxaluria primaria
- Deficiencia de PEPCK
- Atresia yeyunal
- Mucopolisacaridosis tipo III
- Deficiencia de arginina vasopresina
- Sphingosine Phosphate Lyase Insufficiency Syndrome
- Deficiencia de acil-CoA deshidrogenasa de cadena muy larga (LCAD)
- Síndrome de insuficiencia de liasa de fosfato de esfingosina
- Síndrome de Dubin Johnson
