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Results 1 - 10 of 53 for ALCOHOL OR AMMONIA OR BACITRACIN OR BENZETHONIUM OR BENZOCAINE OR IODINE OR LIDOCAINE OR NEOMYCIN OR POLYMYXIN B OR WATER
  1. Cryptogenic cirrhosis 
    ... is not caused by the hepatitis C or B virus or chronic alcohol use. A diagnosis of cryptogenic cirrhosis is typically ...
    https://medlineplus.gov/genetics/condition/cryptogenic-cirrhosis - Genetics
  2. Alcohol use disorder 
    ... TD, Pickering RP, Kerridge BT, Ruan WJ, Huang B, Jung J, Zhang H, Fan A, Hasin DS. Prevalence of 12-Month Alcohol Use, High-Risk Drinking, and DSM-IV Alcohol ...
    https://medlineplus.gov/genetics/condition/alcohol-use-disorder - Genetics
  3. Carbamoyl phosphate synthetase I deficiency 
    ... 2004;27(6):787-8. doi: 10.1023/b:boli.0000045842.59768.ea. Citation on PubMed
    https://medlineplus.gov/...rbamoyl-phosphate-synthetase-i-deficiency - Genetics
  4. Orthostatic hypotension 
    ... factors include heart disease, low blood volume (hypovolemia), alcohol use, ... or drugs that help remove water and salt from the body (diuretics).The non- ...
    https://medlineplus.gov/genetics/condition/orthostatic-hypotension - Genetics
  5. Cholangiocarcinoma 
    ... studied include long-term infection with viral hepatitis B or C, scarring of the liver (cirrhosis), and chronic diseases such as inflammatory bowel disease and diabetes. Researchers suspect that certain lifestyle factors, including smoking, alcohol use, and obesity, may also contribute to the ...
    https://medlineplus.gov/genetics/condition/cholangiocarcinoma - Genetics
  6. Argininosuccinic aciduria 
    ... 10.1023/a:1010560704092. Citation on PubMed Wilcken B, Smith A, Brown DA. Urine screening for ... Citation on PubMed
    https://medlineplus.gov/genetics/condition/argininosuccinic-aciduria - Genetics
  7. Ornithine translocase deficiency 
    ... translocase deficiency is an inherited disorder that causes ammonia and other substances to build up (accumulate) in the blood. Ammonia, which is formed when proteins are broken down ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  8. Arginase deficiency 
    ... acid arginine (a building block of proteins) and ammonia to accumulate gradually in the blood. Ammonia, which is formed when proteins are broken down ... is especially sensitive to the effects of excess ammonia.Arginase deficiency usually becomes evident by about the ...
    https://medlineplus.gov/genetics/condition/arginase-deficiency - Genetics
  9. Pyruvate carboxylase deficiency 
    ... infancy or early childhood.Pyruvate carboxylase deficiency type B has ... buildup of ammonia in the blood (hyperammonemia), and liver failure. They ...
    https://medlineplus.gov/.../pyruvate-carboxylase-deficiency - Genetics
  10. N-acetylglutamate synthase deficiency 
    ... Pauli S, Guffon N, Vianey-Saban C, Wermuth B, Koch HG. Identification of novel mutations ... 2005 Feb 24. Citation on PubMed
    https://medlineplus.gov/.../n-acetylglutamate-synthase-deficiency - Genetics
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