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Results 1 - 10 of 45 for ACETAMINOPHEN OR AMMONIA OR ASPIRIN OR BENZALKONIUM OR DIPHENHYDRAMINE OR IBUPROFEN OR LIDOCAINE
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. Ornithine transcarbamylase deficiency 
    ... transcarbamylase deficiency is an inherited disorder that causes ammonia to accumulate in the blood. Ammonia, which is formed when proteins are broken down ...
    https://medlineplus.gov/.../ornithine-transcarbamylase-deficiency - Genetics
  9. ASNS gene 
    ... other roles. Asparagine helps to break down toxic ammonia within cells, is important for protein modification, and ... this condition. More About This Health Condition aspartate ammonia ligase glutamine-dependent asparagine synthetase TS11 TS11 cell ...
    https://medlineplus.gov/genetics/gene/asns - Genetics
  10. Histidinemia 
    ... gene. HAL deficiency HIS deficiency Histidase deficiency Histidine ammonia-lyase deficiency Histidinuria Hyperhistidinemia Genetic Testing Registry: Histidinemia ...
    https://medlineplus.gov/genetics/condition/histidinemia - Genetics
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