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Results 1 - 10 of 140 for AMMONIA OR ASPIRIN OR BENZALKONIUM OR BENZETHONIUM OR BENZOCAINE OR LIDOCAINE OR WATER
  1. AQP2 gene 
    ... 2. This protein forms a channel that carries water molecules across cell membranes. It is found in ... are a series of small tubes that reabsorb water from the kidneys into the bloodstream.The aquaporin ...
    https://medlineplus.gov/genetics/gene/aqp2 - Genetics
  2. N-acetylglutamate synthase deficiency 
    ... a disorder that causes abnormally high levels of ammonia to accumulate in the blood. Ammonia, which is formed when proteins are broken down ... is especially sensitive to the effects of excess ammonia.The signs and symptoms of N-acetylglutamate synthase ...
    https://medlineplus.gov/.../n-acetylglutamate-synthase-deficiency - Genetics
  3. HMBS gene 
    ... HEM3_HUMAN Hydroxymethylbilane Synthetase PBG-D PBGD Porphobilinogen Ammonia-Lyase Porphobilinogen ammonia-lyase (polymerizing) Porphobilinogen Deaminase Porphyrinogen ...
    https://medlineplus.gov/genetics/gene/hmbs - Genetics
  4. 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
  5. Neurohypophyseal diabetes insipidus 
    Neurohypophyseal diabetes insipidus is a disorder of water balance. The body normally balances fluid intake with the excretion of fluid in urine. However, people with neurohypophyseal diabetes insipidus produce too much ...
    https://medlineplus.gov/.../neurohypophyseal-diabetes-insipidus - Genetics
  6. Argininosuccinic aciduria 
    Argininosuccinic aciduria is an inherited disorder that causes ammonia to accumulate in the blood. Ammonia, which is formed when proteins are broken down ... is especially sensitive to the effects of excess ammonia.Argininosuccinic aciduria usually becomes evident in the first ...
    https://medlineplus.gov/genetics/condition/argininosuccinic-aciduria - Genetics
  7. 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
  8. Nephrogenic diabetes insipidus 
    Nephrogenic diabetes insipidus is a disorder of water balance. The body normally balances fluid intake with the excretion of fluid in urine. However, people with nephrogenic diabetes insipidus produce too much ...
    https://medlineplus.gov/.../condition/nephrogenic-diabetes-insipidus - Genetics
  9. Citrullinemia 
    Citrullinemia is an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. Two types of citrullinemia have been described; they have different signs and symptoms and ...
    https://medlineplus.gov/genetics/condition/citrullinemia - Genetics
  10. Carbamoyl phosphate synthetase I deficiency 
    ... I deficiency is an inherited disorder that causes ammonia to accumulate in the blood (hyperammonemia). Ammonia, which is formed when proteins are broken down ...
    https://medlineplus.gov/...rbamoyl-phosphate-synthetase-i-deficiency - Genetics
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