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Results 1 - 10 of 19 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. 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
  4. 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
  5. Primary carnitine deficiency 
    ... N, Amat di San Filippo C, Pasquali M. Disorders of carnitine transport and the carnitine cycle. Am J Med Genet ... 12. Citation on PubMed Stanley CA. Carnitine deficiency disorders ... I. Carnitine transport: pathophysiology and metabolism of known molecular defects. J ...
    https://medlineplus.gov/.../condition/primary-carnitine-deficiency - Genetics
  6. Carnitine-acylcarnitine translocase deficiency 
    ... N, Amat di San Filippo C, Pasquali M. Disorders of carnitine transport and the carnitine cycle. Am J Med Genet ...
    https://medlineplus.gov/...tine-acylcarnitine-translocase-deficiency - Genetics
  7. Small fiber neuropathy 
    ... conditions cause this disorder. Diabetes mellitus and impaired glucose tolerance are the most common diseases that lead to this disorder, with 6 to ...
    https://medlineplus.gov/genetics/condition/small-fiber-neuropathy - Genetics
  8. Carnitine palmitoyltransferase II deficiency 
    ... N, Amat di San Filippo C, Pasquali M. Disorders of carnitine transport and the carnitine cycle. Am J Med Genet ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  9. Carnitine palmitoyltransferase I deficiency 
    ... N, Amat di San Filippo C, Pasquali M. Disorders of carnitine transport and the carnitine cycle. Am J Med Genet ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  10. Histiocytosis-lymphadenopathy plus syndrome 
    ... R. Human equilibrative nucleoside transporter-3 (hENT3) spectrum disorder mutations impair nucleoside transport, protein localization, and stability. J Biol Chem. 2010 ...
    https://medlineplus.gov/...stiocytosis-lymphadenopathy-plus-syndrome - Genetics
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