Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 8 of 8 for Congenital intestinal transport defect
  1. Chylomicron retention disease 
    ... apolipoprotein B-like protein in intestinal cells Lipid transport defect of intestine Genetic Testing Registry: Chylomicron retention disease Chylomicron retention ...
    https://medlineplus.gov/.../condition/chylomicron-retention-disease - Genetics
  2. Hereditary folate malabsorption 
    ... of the condition. Congenital defect of folate absorption Congenital folate malabsorption Folic acid transport defect Genetic Testing Registry: Congenital defect of folate absorption ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  3. Donnai-Barrow syndrome 
    ... chest cavity (the diaphragm), which is called a congenital diaphragmatic hernia. This potentially serious birth defect allows the stomach and intestines to move into the chest and possibly crowd ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics
  4. Menkes syndrome 
    ... history of the disorder in their family. Copper transport disease Hypocupremia, congenital Kinky hair syndrome Menkea syndrome Menkes disease MK ...
    https://medlineplus.gov/genetics/condition/menkes-syndrome - Genetics
  5. FOLR1 gene 
    ... R, Grosso S, Gartner J. Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed ...
    https://medlineplus.gov/genetics/gene/folr1 - Genetics
  6. Glucose-galactose malabsorption 
    ... them. During the digestion of food, the protein transports the sugars into the cells that line the wall of the intestine (intestinal epithelial cells) as food passes through.The ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  7. SLC5A1 gene 
    ... SGLT1). This protein is found mainly in the intestinal tract and the kidneys. It spans the membrane of cells and moves (transports) two sugars called glucose and galactose from outside ...
    https://medlineplus.gov/genetics/gene/slc5a1 - Genetics
  8. Cutis laxa 
    ... PubMed Kaler SG, DiStasio AT. ATP7A-Related Copper Transport Disorders. 2003 May 9 [updated 2021 Apr 15]. ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics