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Differential Diagnosis For Family history/Metabolic disease

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List of current finding(s):

Metabolic, Storage Disorders
Congenital erythropoetic porphyria
Metabolic disorders
Porphyria variegata
Porphyria, acute intermittent
Chylomicronemia syndrome
Xanthinuria
Coproporphyria erythrohepatica
Citrullinemia/Argininsuccinicaciduria
HyperArgininemia
Phenylketonuria/PKU
LCHAD/Long chain OH-CoA dehydrogenase def
MCAD/Medium chain OH-CoA Dehydrogenase def
Orotic aciduria, hereditary
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Aminoaciduria
Fructose 1,6 diphosphatase deficiency
Fructose intolerance, hereditary
Fructosuria, essential
Galactosemia
Glutaric aciduria/Acidemia
Glutaric aciduria/type II
Hyperglycinuria
Hyperprolinemia
Lesch-Nyhan syndrome
Maple syrup urine disease
Pentosuria, essential
Biochemical Disorders
Hyperammonemia
Hereditary, Familial, Genetic Disorders
Hereditary disorder
Synonyms
DIS METAB, Disease Metabolic, Diseases Metabolic, Disorder metabolic, disorder metabolism, Disorder of metabolism, Disorder of metabolism (disorder), Family history, general metabolic disorder, Generalised metabolic disorder, Generalized metabolic disorder, Generalized metabolic disorder (disorder), MD Metabolic disorders, METAB DIS, Metabolic disease, Metabolic disease (disorder), Metabolic Diseases, Metabolic Disorder, metabolic disorder general, Metabolic disorder unspecified, Metabolic disorders, METABOLIC DISORDERS GENERAL, metabolism disorder, metabolism disorder general, Metabolism Disorders, Thesaurismoses, Thesaurismosis, Unspecified disorder of metabolism
External Links Related to Family history/Metabolic disease
Google
Wikipedia
Merck
Images
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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