Pages that link to "Medicine:Phenylketonuria"
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The following pages link to Medicine:Phenylketonuria:
Displayed 24 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Medicine:Hyperprolinemia (← links)
- Medicine:3-Methylcrotonyl-CoA carboxylase deficiency (← links)
- Medicine:Waardenburg syndrome (← links)
- Medicine:Carnosinemia (← links)
- Medicine:Sarcosinemia (← links)
- Medicine:2-Methylbutyryl-CoA dehydrogenase deficiency (← links)
- Medicine:Ornithine translocase deficiency (← links)
- Medicine:Hartnup disease (← links)
- Medicine:Type I tyrosinemia (← links)
- Medicine:Homocystinuria (← links)
- Medicine:Hawkinsinuria (← links)
- Medicine:2-Hydroxyglutaric aciduria (← links)
- Medicine:Ethylmalonic encephalopathy (← links)
- Medicine:Argininemia (← links)
- Medicine:Fanconi syndrome (← links)
- Medicine:Genetic disorder (← links)
- Medicine:Hyperphenylalaninemia (← links)
- Medicine:List of OMIM disorder codes (← links)
- Medicine:List of genetic disorders (← links)
- Medicine:Microcephaly (← links)
- Medicine:Dopamine-responsive dystonia (← links)
- Medicine:Congenital heart defect (← links)
- Medicine:Segawa Syndrome (← links)
- Medicine:Branched-chain keto acid dehydrogenase kinase deficiency (← links)