| Cardiovascular
|
Aortic arch interruption, hypoplastic left heart syndrome, shock, Fanconi-Albertini-Zellweger syndrome
|
| Chemical / poisoning
|
1,2-Dibromoethane, 4-aminopyridine, aldicarb, ammonium bifluoride, ammonium chloride, aristolochic acid , borates, bromophos, carbaryl, chloralose, chlorfenvinphos, chlorpyrifos, cleistanthus collinus, coumaphos, cyanides, demeton-S-methyl, diazinon, dichlorvos, dicrotophos, dinitrophenol, dioxathion, disulfoton, ethanol, ethion, ethylene glycol, fensulfothion, fenthion, glycol ether, glyphosate, imazapyr, iron compounds, malathion, margosa oil, metaldehyde, methanol, methidathion, methiocarb, methomyl, monochloroacetate, parathion, phenol, phosdrin, polyethylene glycol , profenofos, propoxur, propylene glycol, pyrimidifen, strychnine, terbufos, tetraethyl pyrophosphate, toluene, toxic mushrooms , triethylene Glycol, tungsten, salicylate poisoning, clove
|
| Dermatologic
|
No underlying causes
|
| Drug Side Effect
|
Abacavir, acetazolamide, amitriptyline, amlodipine, amoxapine, amphotericin B, aspirin, cholestyramine, clomipramine, clove, cocaine, desipramine, didanosine, doxepin, emtricitabine, felodipine , imipramine, isoniazid, isradipine, metformin, neuroleptic malignant syndrome, nifedipine, nimodipine, nitroprusside, nortriptyline, paracetamol, phenformin, protriptyline, salicylate poisoning, stavudine, trimipramine, malignant hyperpyrexia, malignant hyperthermia, Reye's syndrome
|
| Ear Nose Throat
|
No underlying causes
|
| Endocrine
|
Adrenal cortex insufficiency, diabetes, diabetic ketoacidosis, glucocorticoid resistance, hyperosmolar non-ketotic diabetic coma, hypoaldosteronism, VIPoma, lipoid congenital adrenal hyperplasia, pseudohypoaldosteronism, 17- beta-hydroxysteroid dehydrogenase deficiency
|
| Environmental
|
No underlying causes
|
| Gastroenterologic
|
Acute liver failure, bacterial overgrowth of small intestine, biliary fistula, congenital chloride diarrhea, diarrhea, duodenal atresia, GI HCO3- loss, hepatic failure, intestinal fistulas, intestinal ischaemia, lactose intolerance, necrotizing enterocolitis, pancreatic fistula, VIPoma, Boichis syndrome
|
| Genetic
|
17- beta-hydroxysteroid dehydrogenase deficiency, 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, 3-hydroxyisobutyric aciduria, 3-methylcrotonyl-CoA carboxylase deficiency, 3-methylglutaconic aciduria, biotinidase deficiency, coenzyme Q10 deficiency, cystinosis, dihydrolipoamide dehydrogenase deficiency, ethylmalonic encephalopathy, Fanconi-Albertini-Zellweger syndrome, fructose-1, 6-diphosphatase deficiency, fructose-1-phosphate aldolase deficiency, galactosemia, glucose transporter type 1 deficiency, glutaric aciduria, glutathione synthase deficiency, glycerol kinase deficiency, glycogenosis, GRACILE syndrome, Hawkinsinuria, hepatocerebral form of mitochondrial DNA depletion syndrome, HMG-CoA lyase deficiency, holocarboxylase synthase deficiency, isovaleric acidaemia, lipoid congenital adrenal hyperplasia, long chain hydroxyacyl-CoA dehydrogenase deficiency, Lowe Syndrome, Lutz-Richner and Landolt syndrome, malignant hyperpyrexia, malignant hyperthermia, malonyl-CoA decarboxylase deficiency, maple syrup urine disease, medium chain acyl-CoA dehydrogenase deficiency, medullary cystic kidney disease, MELAS, MERRF, methylmalonic acidemia, microcephaly, Amish type, mitochondrial acetoacetyl-CoA thiolase deficiency, mitochondrial aspartyl-tRNA synthetase deficiency, molybdenum cofactor deficiency, myopathy with deficiency of succinate dehydrogenase and aconitase, nephronophthisis, phosphoglucomutase deficiency, propionic acidemia, propionyl-CoA carboxylase deficiency, pseudohypoaldosteronism, pyruvate carboxylase deficiency, pyruvate dehydrogenase deficiency, Senior-Loken Syndrome, short-chain acyl-coenzyme A dehydrogenase deficiency, succinyl-CoA acetoacetate transferase deficiency, succinyl-CoA synthetase deficiency, vitamin B12-responsive methylmalonic acidemia, congenital chloride diarrhea, osteopetrosis with renal tubular acidosis
|
| Hematologic
|
Myeloma
|
| Iatrogenic
|
Hyperalimentation, Reye's Syndrome, short bowel syndrome, ureterosigmoidostomy, ureteral diversion, malignant hyperpyrexia, malignant hyperthermia
|
| Infectious Disease
|
No underlying causes
|
| Musculoskeletal / Ortho
|
Osteopetrosis with renal tubular acidosis, myopathy with deficiency of succinate dehydrogenase and aconitase
|
| Neurologic
|
Leigh syndrome, Lowe Syndrome, microcephaly, Amish type
|
| Nutritional / Metabolic
|
Hyperkalaemia, hypoalbuminism, ketoacidosis, lactic acidosis, organic acidemia, diabetic ketoacidosis, hyperosmolar non-ketotic diabetic coma, 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, 3-hydroxyisobutyric aciduria, 3-methylcrotonyl-CoA carboxylase deficiency, 3-methylglutaconic aciduria, biotinidase deficiency, coenzyme Q10 deficiency, cystinosis, dihydrolipoamide dehydrogenase deficiency, ethylmalonic encephalopathy, fructose-1, 6-diphosphatase deficiency, fructose-1-phosphate aldolase deficiency, galactosemia, glutaric aciduria, glutathione synthase deficiency, glycerol kinase deficiency, glycogenosis, Hawkinsinuria, HMG-CoA lyase deficiency, holocarboxylase synthase deficiency, isovaleric acidaemia, long chain hydroxyacyl-CoA dehydrogenase deficiency, malonyl-CoA decarboxylase deficiency, maple syrup urine disease, medium chain acyl-CoA dehydrogenase deficiency, methylmalonic acidemia, mitochondrial acetoacetyl-CoA thiolase deficiency, molybdenum cofactor deficiency, myopathy with deficiency of succinate dehydrogenase and aconitase,phosphoglucomutase deficiency, propionic acidemia, propionyl-CoA carboxylase deficiency, pyruvate carboxylase deficiency, pyruvate dehydrogenase deficiency, short-chain acyl-coenzyme A dehydrogenase deficiency, succinyl-CoA acetoacetate transferase deficiency, succinyl-CoA synthetase deficiency, vitamin B12-responsive methylmalonic acidemia, Leigh syndrome, Fanconi-Albertini-Zellweger syndrome, 17- beta-hydroxysteroid dehydrogenase deficiency
|
| Obstetric/Gynecologic
|
No underlying causes
|
| Oncologic
|
Myeloma
|
| Opthalmologic
|
Lowe Syndrome, Senior-Loken Syndrome
|
| Overdose / Toxicity
|
Abacavir, acetazolamide, amitriptyline, amlodipine, amoxapine, amphotericin B, aspirin, cholestyramine, clomipramine, clove, cocaine, desipramine, didanosine, doxepin, emtricitabine, felodipine , imipramine, isoniazid, isradipine, metformin, neuroleptic malignant syndrome, nifedipine, nimodipine, nitroprusside, nortriptyline, paracetamol, phenformin, protriptyline, salicylate poisoning, stavudine, trimipramine, malignant hyperpyrexia, malignant hyperthermia, Reye's syndrome
|
| Psychiatric
|
No underlying causes
|
| Pulmonary
|
No underlying causes
|
| Renal / Electrolyte
|
Acute renal failure, analgesic nephropathy syndrome, Boichis syndrome, chronic interstitial nephritis, chronic renal failure, compensation in primary respiratory alkalosis, Lightwood Albright syndrome, renal HCO3- loss, Renal tubular acidosis, Lowe Syndrome, Senior-Loken Syndrome, hypoaldosteronism, medullary cystic kidney disease, nephronophthisis, Ureteral diversion, osteopetrosis with renal tubular acidosis
|
| Rheum / Immune / Allergy
|
No underlying causes
|
| Sexual
|
17- beta-hydroxysteroid dehydrogenase deficiency
|
| Trauma
|
No underlying causes
|
| Urologic
|
Ureteral diversion
|
| Dental
|
No underlying causes
|
| Miscellaneous
|
Cuffed blood sample, near-drowning, starvation
|
