Pages that link to "Ornithine transcarbamylase deficiency"
Jump to navigation
Jump to search
The following pages link to Ornithine transcarbamylase deficiency:
Displaying 36 items.
- ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases (← links)
- Inborn errors of renal tubular transport (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Hawkinsinuria (← links)
- Inborn errors of amino acid metabolism (← links)
- D-Glyceric acidemia (← links)
- Urocanic aciduria (← links)
- Amino acid transport disorder (← links)
- Argininemia (← links)
- 2-Hydroxyglutaric aciduria (← links)
- Hyper-IgM syndrome type 1 (← links)
- IPEX (syndrome) (← links)
- X-Linked mental retardation (← links)
- Focal dermal hypoplasia (← links)
- CHILD (← links)
- OTCD (redirect page) (← links)
- Type I tyrosinemia (← links)
- Type II tyrosinemia (← links)
- Type III tyrosinemia (← links)
- Glycogen storage disease type IX (← links)
- WikiPatient: Metabolic Disease (← links)
- Viral encephalitis causes (← links)
- Pedal edema causes (← links)
- Disequilibrium causes (← links)
- WBR0976 (← links)
- Hyperthermia causes (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Encephalitis (← links)
- Sandbox:Mental retardation causes (← links)
- Template:Metabolic pathway (← links)
- Template:Metabolic pathology (← links)
- Template:Amino acid metabolic pathology (← links)
- Template:X-linked disorders (← links)