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Results 1 - 10 of 327 for Low
  1. Familial HDL deficiency 
    Familial HDL deficiency is a condition characterized by low levels of high-density lipoprotei% (HDL) in the ... or phospholipids available to form HDL, resulting in low levels of HDL in the blood. A shortage ( ...
    https://medlineplus.gov/genetics/condition/familial-hdl-deficiency - Genetics
  2. Autosomal dominant hypocalcemia 
    Autosomal dominant hypocalcemia is characterized by low levels of calcium in the blood (hypocalcemia). Affected individuals can have an imbalance of other molecules in the blood as well, including ...
    https://medlineplus.gov/.../autosomal-dominant-hypocalcemia - Genetics
  3. Acatalasemia 
    Acatalasemia is a condition characterized by very low levels of an enzyme called catalase. Many people with acatalasemia never have any health problems related to the condition and are diagnosed because ...
    https://medlineplus.gov/genetics/condition/acatalasemia - Genetics
  4. Fundus albipunctatus 
    ... characterized by an impaired ability to see in low light (night blindness) and the presence of whitish- ... stimulated, and vision is impaired.For vision in low-light conditions, the eyes primarily use 11-cis ...
    https://medlineplus.gov/genetics/condition/fundus-albipunctatus - Genetics
  5. Imerslund-Gräsbeck syndrome 
    Imerslund-Gräsbeck syndrome is a condition caused by low levels of vitamin B12 (also known as cobalamin). ... of red blood cells, leading to megaloblastic anemia. Low levels of vitamin B12 can also affect the ...
    https://medlineplus.gov/.../condition/imerslund-grasbeck-syndrome - Genetics
  6. Warfarin sensitivity 
    ... is a condition in which individuals have a low tolerance for the drug warfarin. Warfarin is an ... slower than average and can be stopped by low warfarin doses. If people with warfarin sensitivity take ...
    https://medlineplus.gov/genetics/condition/warfarin-sensitivity - Genetics
  7. Progressive familial intrahepatic cholestasis 
    ... deafness, diarrhea, inflammation of the pancreas (pancreatitis), and low levels of fat-soluble vitamins (vitamins A, D, ... BSEP deficiency Byler disease Byler syndrome FIC1 deficiency Low γ-GT familial intrahepatic cholestasis MDR3 deficiency Genetic ...
    https://medlineplus.gov/...ressive-familial-intrahepatic-cholestasis - Genetics
  8. Benign recurrent intrahepatic cholestasis 
    ... related intrahepatic cholestasis ATP8B1-related intrahepatic cholestasis BRIC Low gamma-GT familial intrahepatic cholestasis Recurrent familial intrahepatic ...
    https://medlineplus.gov/...benign-recurrent-intrahepatic-cholestasis - Genetics
  9. Hereditary hypophosphatemic rickets 
    Hereditary hypophosphatemic rickets is a disorder related to low levels of phosphate in the blood (hypophosphatemia). Phosphate ...
    https://medlineplus.gov/.../hereditary-hypophosphatemic-rickets - Genetics
  10. 17q12 deletion syndrome 
    17q12 deletion syndrome is a condition that results from the deletion of a small piece of chromosome 17 in each cell. The deletion occurs on the long (q) arm ...
    https://medlineplus.gov/genetics/condition/17q12-deletion-syndrome - Genetics
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