Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Disorders of amino acid absorption or transport (Q40010) (← links)
- Cystinuria (Q40011) (← links)
- Oculocerebrorenal syndrome (Q40012) (← links)
- Cystinosis (Q40013) (← links)
- Disorders of methionine cycle or sulphur amino acid metabolism (Q40014) (← links)
- Argininosuccinic aciduria (Q40015) (← links)
- Disorders of urea cycle metabolism (Q40016) (← links)
- Argininaemia (Q40017) (← links)
- Carbamoylphosphate synthetase deficiency (Q40018) (← links)
- Citrullinaemia (Q40019) (← links)
- Disorders of lysine or hydroxylysine metabolism (Q40020) (← links)
- Disorders of ornithine metabolism (Q40021) (← links)
- Disorders of glycine metabolism (Q40022) (← links)
- Glycine encephalopathy (Q40023) (← links)
- Sarcosinaemia (Q40024) (← links)
- Disorders of proline or hydroxyproline metabolism (Q40025) (← links)
- Disorders of beta or omega amino acid metabolism (Q40026) (← links)
- Disorders of creatine metabolism (Q40027) (← links)
- Prolidase deficiency (Q40028) (← links)
- Disorders of serine metabolism (Q40029) (← links)
- Homocarnosinosis (Q40030) (← links)
- Disorders of the gamma-glutamyl cycle (Q40031) (← links)
- Aminoaciduria (Q40032) (← links)
- Congenital lactase deficiency (Q40033) (← links)
- Secondary lactase deficiency (Q40034) (← links)
- Lactose intolerance (Q40035) (← links)
- Primary lactase deficiency (Q40036) (← links)
- Glycogen storage disease (Q40037) (← links)
- Hereditary fructose intolerance (Q40038) (← links)
- Disorders of fructose metabolism (Q40039) (← links)
- Fructose malabsorption (Q40040) (← links)
- Galactokinase deficiency (Q40041) (← links)
- Disorders of galactose metabolism (Q40042) (← links)
- Glucose or galactose intolerance of newborn (Q40043) (← links)
- Galactose-1-phosphate uridyltransferase deficiency (Q40044) (← links)
- Acquired monosaccharide malabsorption (Q40045) (← links)
- Glucose-galactose malabsorption (Q40046) (← links)
- Congenital sucrase-isomaltase deficiency (Q40047) (← links)
- Maltase-glucoamylase deficiency (Q40048) (← links)
- Disorders of pyruvate metabolism (Q40049) (← links)
- Pyruvate dehydrogenase complex deficiency (Q40050) (← links)
- Pyruvate kinase deficiency (Q40051) (← links)
- Pyruvate carboxylase deficiency (Q40052) (← links)
- Lactate dehydrogenase deficiency (Q40053) (← links)
- Disorders of facilitated glucose transport (Q40054) (← links)
- Alpha, alpha trehalase deficiency (Q40055) (← links)
- Renal glycosuria (Q40056) (← links)
- Disorders of the pentose phosphate pathway (Q40057) (← links)
- Disorders of glycerol metabolism (Q40058) (← links)
- Inborn errors of carbohydrate metabolism (Q40059) (← links)
