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Differential Diagnosis For Episodic symptoms/events: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetes mellitus, poorly controlled
Gouty attack, acute/podagra
Diabetes mellitus
Diabetic autonomic neuropathy syndrome
Lactose intolerance
Primary lactic acidemia/children
Glucose 6 PD deficiency
Porphyria, acute intermittent
Pseudogout syndrome
Diabetic diarrhea syndrome
Coproporphyria erythrohepatica
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Ketotic hyperglycinemia, idiopathic
Methyl crotonyl CoA carboxylase deficiency
Methylmalonic acidemia/ketotic glycine
Propionicacidemia/ketotic glycinemia
Pyruvate carboxylase enzyme deficiency/PCD
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Infantile mitochondrial myopathy/Cox defect
Alphamethylacetoacetate accumulation
LCHAD/Long chain OH-CoA dehydrogenase def
MCAD/Medium chain OH-CoA Dehydrogenase def
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Adult ceroid lipofuscinosis/Kufs
Alkaptonuria/Ochronosis
Cystinuria
Fructose intolerance, hereditary
Glutaric aciduria/type II
Hartnup disease
McArdle's syndrome
Urea cycle/metabolic disorder
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