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Results 1 - 10 of 59 for Glucose transport disorder
  1. Glycogen storage disease type I 
    ... disease Von Gierke's disease Genetic Testing Registry: Glucose-6-phosphate transport defect Genetic Testing Registry: Glycogen storage disease due to glucose-6-phosphatase deficiency type IA ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-i - Genetics
  2. GLUT1 deficiency syndrome 
    ... signs and symptoms of the condition. De Vivo disease Encephalopathy due to GLUT1 deficiency G1D Glucose transport defect, blood-brain barrier Glucose transporter protein syndrome ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  3. SLC2A1 gene 
    ... on PubMed Guo X, Geng M, Du G. Glucose transporter 1, distribution in the brain and in neural disorders: its relationship with transport of neuroactive drugs through the blood-brain barrier. ...
    https://medlineplus.gov/genetics/gene/slc2a1 - Genetics
  4. SLC37A4 gene 
    ... gene have been found to cause glycogen storage disease type Ib (GSDIb). ... prevent the transport of glucose 6-phosphate to the endoplasmic reticulum. ...
    https://medlineplus.gov/genetics/gene/slc37a4 - Genetics
  5. Glucose-galactose malabsorption 
    ... Alhunaitti H, Bin-Taleb YY, Alhussaini BH. Congenital glucose-galactose ... sugar transport in health and disease. J Intern Med. 2007 Jan;261(1):32- ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  6. G6PC1 gene 
    The G6PC1 gene provides instructions for making an enzyme called glucose 6-phosphatase. This enzyme is found on the membrane of the endoplasmic reticulum, ...
    https://medlineplus.gov/genetics/gene/g6pc1 - Genetics
  7. POGLUT1 gene 
    The POGLUT1 gene provides instructions for making a protein called protein O-glucosyltransferase 1. This protein is located in a cell structure called the ...
    https://medlineplus.gov/genetics/gene/poglut1 - Genetics
  8. ENPP1 gene 
    ... resulting impairment of ENPP1's role in melanin transport and keratinocyte ... More About This Health Condition More than ...
    https://medlineplus.gov/genetics/gene/enpp1 - Genetics
  9. Cole disease 
    ... resulting impairment of ENPP1's role in melanin transport and keratinocyte development leads to the ... This condition is inherited in an ...
    https://medlineplus.gov/genetics/condition/cole-disease - Genetics
  10. SLC5A1 gene 
    ... SGLT1 protein, and a similar protein called SGLT2, transport glucose from proximal tubules, ensuring that the sugar is ... short.The altered SGLT1 protein's ability to transport glucose and galactose is reduced or absent. The sugars ...
    https://medlineplus.gov/genetics/gene/slc5a1 - Genetics
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