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Possible Causes For Acidosis - Causes: Metabolic, Storage Disorders
List of current finding(s):
Acidosis - Causes
- Trauma Causes (2)
- Electromagnetic, Physics, trauma, Radiation Causes (5)
- Iatrogenic, Self Induced Disorders (2)
- Surgical, Procedure Complication (3)
- Infectious Disorders (Specific Agent) (4)
- Infected organ, Abscesses (3)
- Granulomatous, Inflammatory Disorders (1)
- Neoplastic Disorders (1)
- Allergic, Collagen, Auto-Immune Disorders (4)
- Metabolic, Storage Disorders (40)
- Biochemical Disorders (13)
- Deficiency Disorders (5)
- Congenital, Developmental Disorders (4)
- Hereditary, Familial, Genetic Disorders (6)
- Anatomic, Foreign Body, Structural Disorders (6)
- Arteriosclerotic, Vascular, Venous Disorders (5)
- Functional, Physiologic Variant Disorders (1)
- Vegetative, Autonomic, Endocrine Disorders (8)
- Reference to Organ System (11)
- Pathophysiologic (2)
- Drugs (23)
- Poisoning (Specific Agent) (25)
- Organ Poisoning (Intoxication) (1)
- Synonyms (2)
- Definition
- External Links Related to Acidosis - Causes
- Metabolic, Storage Disorders:
- 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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