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Results 1 - 10 of 13 for Glucose intolerance
  1. Glucose-galactose malabsorption 
    ... the condition. Carbohydrate intolerance Complex carbohydrate intolerance Congenital glucose-galactose intolerance Congenital glucose-galactose malabsorption GGM Monosaccharide malabsorption Genetic ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  2. ALDOB gene 
    ... The combination of decreased cellular energy, low blood glucose, and liver cell death leads to the features of hereditary fructose intolerance. More About This Health Condition ALDB ALDO2 ALDOB_ ...
    https://medlineplus.gov/genetics/gene/aldob - Genetics
  3. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... Alpha-1 antitrypsin deficiency Celiac disease Familial ... Cheek dimples Eye color Hair texture Hair color ( ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  4. Mitochondrial DNA 
    ... do not produce enough insulin to regulate blood glucose effectively. Researchers have ... intolerance). More severely affected individuals may have problems with ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  5. LCT gene 
    ... the small intestine and causing severe diarrhea.Lactose intolerance in adulthood can also be caused by the ... Diekmann L, Pfeiffer K, Naim HY. Congenital lactose intolerance is triggered by severe mutations on both alleles ...
    https://medlineplus.gov/genetics/gene/lct - Genetics
  6. Congenital sucrase-isomaltase deficiency 
    ... signs and symptoms of the condition. Congenital sucrose intolerance Congenital sucrose-isomaltose malabsorption CSID Disaccharide intolerance I SI deficiency Sucrase-isomaltase deficiency Genetic Testing ...
    https://medlineplus.gov/.../congenital-sucrase-isomaltase-deficiency - Genetics
  7. Glycogen storage disease type IX 
    ... muscle pain, and cramps, especially during exercise (exercise intolerance). Most affected individuals have muscle weakness that worsens ... of cellular energy is a simple sugar called glucose. Glucose is stored in muscle and liver cells ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-ix - Genetics
  8. Glycogen storage disease type 0 
    ... P, Oldfors A, Holme E. Cardiomyopathy and exercise intolerance in muscle glycogen storage disease 0. N Engl ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  9. MT-TL1 gene 
    ... pain, and extreme fatigue, particularly during exercise (exercise intolerance). In some cases, the heart muscle is also ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  10. Mitochondrial complex III deficiency 
    ... and extreme tiredness (fatigue), particularly during exercise (exercise intolerance). More severely affected individuals have problems with multiple ... Lach B, Morgan-Hughes J, DiMauro S. Exercise intolerance due to mutations in the cytochrome b gene ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
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