Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 11 - 20 of 80 for acidosis
  1. ATP6V0A4 gene 
    ... have been identified in people with renal tubular acidosis with deafness, a disorder involving excess acid in the blood (metabolic acidosis), bone weakness, and hearing loss caused by changes ...
    https://medlineplus.gov/genetics/gene/atp6v0a4 - Genetics
  2. Dihydrolipoamide dehydrogenase deficiency 
    ... threatening buildup of lactic acid in tissues (lactic acidosis), which can cause nausea, vomiting, severe breathing problems, ... the body, damaging tissues and leading to lactic acidosis and other chemical imbalances. In addition, the production ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
  3. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 
    ... cause the blood to become too acidic (metabolic acidosis). If untreated, the disorder can lead to breathing ... byproducts called organic acids can result in metabolic acidosis. A shortage of ketones often leads to hypoglycemia. ...
    https://medlineplus.gov/...oxy-3-methylglutaryl-coa-lyase-deficiency - Genetics
  4. Pseudohypoaldosteronism type 2 
    ... high levels of chloride (hyperchloremia) and acid (metabolic acidosis) in their blood (together, referred to as hyperchloremic metabolic acidosis). People with hyperkalemia, hyperchloremia, and metabolic acidosis can ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-2 - Genetics
  5. Pseudohypoaldosteronism type 1 
    ... high levels of acid in the blood (metabolic acidosis). Hyponatremia, hyperkalemia, or metabolic acidosis can cause nonspecific symptoms such as nausea, vomiting, ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-1 - Genetics
  6. MT-TV gene 
    ... a very rare cause of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). Most cases of ... G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes. Neurology. 1998 Jan;50( ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  7. MT-TH gene 
    ... people with the features of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) have a mutation ... tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS). Mitochondrion. 2011 Sep; ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
  8. DLD gene 
    ... buildup of lactic acid in the tissues (lactic acidosis), neurological problems, and liver disease.Most DLD mutations ... chemical reaction to lactic acid, contributing to lactic acidosis in affected individuals. Impairment of αKGDH leads to ...
    https://medlineplus.gov/genetics/gene/dld - Genetics
  9. PDHA1 gene 
    ... chemical called lactic acid in the body (lactic acidosis), delayed development, and neurological problems. Dozens of PDHA1 ... another chemical reaction, to lactic acid, causing lactic acidosis. In addition, the production of cellular energy is ...
    https://medlineplus.gov/genetics/gene/pdha1 - Genetics
  10. PDHB gene 
    ... chemical called lactic acid in the body (lactic acidosis), delayed development, and neurological problems. These mutations change ... another chemical reaction, to lactic acid, causing lactic acidosis. In addition, the production of cellular energy is ...
    https://medlineplus.gov/genetics/gene/pdhb - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · next