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 - 10 of 14 for Carbohydrate transport disease
  1. Hereditary fructose intolerance 
    ... Elsevier; 2020:chap 105. Mojica A, Weinstock RS. Carbohydrates. In: ... Disease . 8th ed. Philadelphia, PA: Elsevier; 2023:chap 37.
    https://medlineplus.gov/ency/article/000359.htm - Medical Encyclopedia
  2. Acute Intermittent Porphyria (AIP) (American Porphyria Foundation)  
    Porphyria/Specifics ... Porphyria ... American Porphyria Foundation
    https://porphyriafoundation.org/for-patients/types-of-porphyria/aip - External Health Links
  3. Glucose-galactose malabsorption 
    ... Wright EM, Hirayama BA, Loo DF. Active sugar transport in health and disease. J Intern Med. 2007 Jan;261(1):32- ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  4. Riboflavin transporter deficiency neuronopathy 
    ... are also involved in the breakdown (metabolism) of carbohydrates, fats, and proteins.Mutations in the SLC52A2 or SLC52A3 gene lead to an abnormal riboflavin transporter protein with impaired ability to transport riboflavin. Consequently, there is a reduction of riboflavin ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  5. SLC52A2 gene 
    ... are also involved in the breakdown (metabolism) of carbohydrates, fats, and proteins. ... Laere syndrome and Fazio-Londe disease. Some of the gene mutations involved in riboflavin ...
    https://medlineplus.gov/genetics/gene/slc52a2 - Genetics
  6. SLC52A3 gene 
    ... are also involved in the breakdown (metabolism) of carbohydrates, fats, and proteins. ... syndrome and Fazio-Londe disease. The gene mutations involved in this condition lead ...
    https://medlineplus.gov/genetics/gene/slc52a3 - Genetics
  7. COG5-congenital disorder of glycosylation 
    ... not show signs and symptoms of the condition. Carbohydrate deficient glycoprotein syndrome type IIi CDG IIi CDG2I ...
    https://medlineplus.gov/...cog5-congenital-disorder-of-glycosylation - Genetics
  8. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF ... muscular dystrophy; exercise with a disability; neuromuscular ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links
  9. SLC5A1 gene 
    ... It spans the membrane of cells and moves (transports) two sugars called ... in milk) and carbohydrates in the diet during digestion.In the intestinal ...
    https://medlineplus.gov/genetics/gene/slc5a1 - Genetics
  10. Hypokalemic periodic paralysis 
    ... viral illness, or certain medications. Often, a large, carbohydrate-rich meal or vigorous exercise in the evening ... ions. The channel formed by the CACNA1S protein transports calcium ions into cells, while the channel formed ...
    https://medlineplus.gov/.../condition/hypokalemic-periodic-paralysis - Genetics
previous · 1 · 2 · next