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Possible Causes For Acidosis - Causes: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetes mellitus, poorly controlled
Diabetic ketoacidosis/coma
Renal tubular disorders/metabolic
Primary lactic acidemia/children
Fanconi's syndrome, adult (acquired)
Fanconi's Hereditary Renal Disease
Renal tubular acidosis type IV
Combined carboxylase/Biotinidase deficiency
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Hydroxybutyric acidemia
Ketotic hyperglycinemia, idiopathic
Methylmalonic acidemia/ketotic glycine
Mitochondrial respiratory chain defects
Propionicacidemia/ketotic glycinemia
Pyroglutamic acidemia
Pyruvate carboxylase enzyme deficiency/PCD
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Infantile mitochondrial myopathy/Cox defect
Acyl-CoA Dehydrogenase/short chain def
Alphamethylacetoacetate accumulation
Beta-hydroxyisolvaleric acidemia
Carbamoyl phosphate synthetase defic
Glutamic acidemia
Hyperglycinemia, ketotic
LCHAD/Long chain OH-CoA dehydrogenase def
Orotic aciduria, hereditary
Proprionic acidemia/congenital
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Cystinuria
Fructose intolerance, hereditary
Galactosemia
Glutaric aciduria/Acidemia
Glycogen storage diseases
Hyperglycinuria
Phosphoenolpyruvate carboxykinase defic (PEPCK)
Pipecolic acidemia
Von Gierke's disease/glycogenosis I
Organic acidemias/Metabolic syndromes
Renal tubular acidosis acquired
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