What can cause metabolic acidosis?

Cocaine 2-acetylaminofluorene hyperkalemia cyanide poisoning drowning malignant hyperthermia galactosemia Medium chain acyl-CoA dehydrogenase deficiency Sodium nitroprusside Propionic acidemia Pseudohypoaldosteronism type 1, autosomal recessive glutathione synthetase deficiency 3-methylcrotonyl-CoA carboxylase deficiency glutaric acidemia type 2 Beta-ketothiolase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Hawkinsinuria biotinidase deficiency ethanol neuroleptic malignant syndrome Acute tubular necrosis short bowel syndrome Glycerol kinase deficiency Thiosulfate Short chain acyl-CoA dehydrogenase deficiency Formic acid Long chain hydroxyacyl-CoA dehydrogenase deficiency Iron compounds Adrenal cortex insufficiency.

Pseudohypoaldosteronism type 1, autosomal recessive Pseudohypoaldosteronism type 1, autosomal recessive Pseudohypoaldosteronism, the condition that mimics hypoaldosteronism wikipedia glutathione synthetase deficiency glutathione synthetase deficiency glutathione synthetase deficiency, a rare, autosomal recessive metabolic disorder that prevents the production of glutathione wikipedia 3-methylcrotonyl-CoA carboxylase deficiency 3-methylcrotonyl-CoA carboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency, also known as 3-Methylcrotonylglycinuria type 1 or BMCC deficiency, an inherited disorder in which the body is unable to process certain proteins properly wikipedia glutaric acidemia type 2 glutaric acidemia type 2 Glutaric acidemia type 2, an autosomal recessive metabolic disorder that is characterised by defects in the ability of the body to use proteins and fats for energy wikipedia Beta-ketothiolase deficiency Beta-ketothiolase deficiency Beta-ketothiolase deficiency, a rare, autosomal recessive metabolic disorder in which the body cannot properly process the amino acid isoleucine or the products of lipid breakdown wikipedia 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency also referred to as HMG-CoA lyase deficiency or Hydroxymethylglutaric aciduria, an uncommon inherited disorder in which the body cannot properly process the amino acid leucine wikipedia Hawkinsinuria Hawkinsinuria Hawkinsinuria, also called 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, an autosomal dominant metabolic disorder affecting the metabolism of the sulfur amino acid hawkinsin wikipedia biotinidase deficiency biotinidase deficiency biotinidase deficiency, an autosomal recessive metabolic disorder in which the body is not able to process the nutrient biotin properly ethanol ethanol, the alcohol found in alcoholic beverages, also known as ethyl alcohol or grain alcohol wikipedia neuroleptic malignant syndrome neuroleptic malignant syndrome, a life-threatening, neurological disorder most often caused by an adverse reaction to neuroleptic or antipsychotic drugs wikipedia Acute tubular necrosis Acute tubular necrosis or, a medical condition involving the death of tubular cells that form the tubule that transports urine to the ureters while reabsorbing 99% of the water wikipedia short bowel syndrome short bowel syndrome, a malabsorption disorder caused by the surgical removal of the small intestine, or rarely due to the complete dysfunction of a large segment of bowel wikipedia Glycerol kinase deficiency Hyperglycerolemia, also referred to as "glycerol kinase deficiency", "gk deficiency", "gkd", and "gk1 deficiency", the condition characterized by high levels of glycerides, including monoglycerides, diglycerides and triglycerides, in the blood stream wikipedia Thiosulfate Thiosulfate, the chemical compound, a cause of the phenomenon edema and metabolic acidosis Short chain acyl-CoA dehydrogenase deficiency Short chain acyl-CoA dehydrogenase deficiency, the cause and medical concept with DiseasesDB code "31599" Formic acid Formic acid, the chemical compound, a cause of the phenomenon dementia and lung cancer Long chain hydroxyacyl-CoA dehydrogenase deficiency Long chain hydroxyacyl-CoA dehydrogenase deficiency, the cause and medical concept with DiseasesDB code "29848" Iron compounds Iron compounds (inorganic or organic compounds containing trivalent iron) Adrenal cortex insufficiency Adrenal cortex insufficiency (abnormally diminished activity of the adrenal gland).

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