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Differential Diagnosis For pH, arterial blood (Lab) - Increased: Metabolic, Storage Disorders
List of current finding(s):
pH, arterial blood (Lab) - Increased
- Electromagnetic, Physics, trauma, Radiation Causes (6)
- Iatrogenic, Self Induced Disorders (4)
- Surgical, Procedure Complication (1)
- Infectious Disorders (Specific Agent) (6)
- Infected organ, Abscesses (2)
- Granulomatous, Inflammatory Disorders (3)
- Neoplastic Disorders (2)
- Allergic, Collagen, Auto-Immune Disorders (5)
- Metabolic, Storage Disorders (16)
- Biochemical Disorders (8)
- Deficiency Disorders (1)
- Congenital, Developmental Disorders (1)
- Hereditary, Familial, Genetic Disorders (5)
- Usage, Degenerative, Necrosis, Age Related Disorders (1)
- Relational, Mental, Psychiatric Disorders (6)
- Anatomic, Foreign Body, Structural Disorders (5)
- Arteriosclerotic, Vascular, Venous Disorders (1)
- Functional, Physiologic Variant Disorders (5)
- Vegetative, Autonomic, Endocrine Disorders (14)
- Reference to Organ System (7)
- Pathophysiologic (3)
- Drugs (16)
- Poisoning (Specific Agent) (14)
- Organ Poisoning (Intoxication) (1)
- Synonyms (2)
- Definition
- External Links Related to pH, arterial blood (Lab) - Increased
- Metabolic, Storage Disorders:
- Fanconi's syndrome, adult (acquired)
- Porphyria, acute intermittent
- Combined carboxylase/Biotinidase deficiency
- Methylmalonic acidemia/ketotic glycine
- Propionicacidemia/ketotic glycinemia
- Pyroglutamic acidemia
- Acyl-CoA Dehydrogenase/short chain def
- Alphamethylacetoacetate accumulation
- Carbamoyl phosphate synthetase defic
- Hyperglycinemia, ketotic
- LCHAD/Long chain OH-CoA dehydrogenase def
- Proprionic acidemia/congenital
- VLCHAD/Very Long chain OH-CoA dehydrogenase def
- Forbes disease (Cori disease, III)
- Fructose intolerance, hereditary
- McArdle's syndrome
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