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Differential Diagnosis For pH, arterial blood (Lab) - Increased: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
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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