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Results 1 - 10 of 1,873 for Deficiency
  1. G6PD Deficiency (National Library of Medicine)  
    Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder that is most common in males. About 1 in 10 African American males in the United States ...
  2. Hemophilia (National Library of Medicine)  
    What is hemophilia? Hemophilia is a rare bleeding disorder in which the blood does not clot properly. This can lead to problems with bleeding too much ...
  3. Alpha-1 Antitrypsin Deficiency (National Library of Medicine)  
    What is alpha-1 antitrypsin deficiency (AAT deficiency)? Alpha-1 antitrypsin deficiency (AAT deficiency, or AATD) is an inherited condition that raises your risk for lung and ...
  4. Vitamin D Deficiency (National Library of Medicine)  
    What is vitamin D deficiency? Vitamin D deficiency means that your body is not getting enough vitamin D to stay healthy. Why do I need vitamin D and how do I ...
  5. Lactose Intolerance (National Library of Medicine)  
    Lactose intolerance means that you cannot digest foods with lactose in them. Lactose is the sugar found in milk and foods made with milk. After eating foods ...
  6. Complete plasminogen activator inhibitor 1 deficiency (complete PAI-1 deficiency) is a disorder that causes abnormal bleeding. In people with this disorder, bleeding ...
  7. 3-beta (β)-hydroxysteroid dehydrogenase (HSD) deficiency is an inherited disorder that affects hormone-producing glands including the gonads (ovaries in females ...
  8. GABA-transaminase deficiency is a brain disease (encephalopathy) that begins in infancy. Babies with this disorder have recurrent seizures (epilepsy), uncontrolled ...
  9. 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins. ...
  10. 3-hydroxyacyl-CoA dehydrogenase deficiency is an inherited condition that prevents the body from converting certain fats to energy, particularly during ...
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