Pages that link to "Property:P68"
From determinar.ia.br - Determine suas informações
The following pages link to Canonical URI (P68):
Displaying 50 items.
- Sequelae of protein-energy malnutrition (Q39959) (← links)
- Sequelae of vitamin C deficiency (Q39960) (← links)
- Localised adiposity (Q39961) (← links)
- Overweight or localised adiposity (Q39963) (← links)
- Obesity (Q39964) (← links)
- Obesity in adults (Q39965) (← links)
- Obesity due to energy imbalance (Q39966) (← links)
- Obesity in children or adolescents (Q39967) (← links)
- Drug-induced obesity (Q39968) (← links)
- Obesity hypoventilation syndrome (Q39969) (← links)
- Overweight in adults (Q39970) (← links)
- Overweight in infants, children or adolescents (Q39971) (← links)
- Overweight (Q39972) (← links)
- Mineral excesses (Q39973) (← links)
- Hypercalcaemia (Q39974) (← links)
- Vitamin excesses (Q39975) (← links)
- Hypervitaminosis A (Q39976) (← links)
- Hypercarotenaemia (Q39977) (← links)
- Megavitamin-B6 syndrome (Q39978) (← links)
- Hypervitaminosis D (Q39979) (← links)
- Manganese excess (Q39980) (← links)
- Aluminium excess (Q39981) (← links)
- Sodium chloride excess (Q39982) (← links)
- Zinc excess (Q39983) (← links)
- Fluorine excess (Q39984) (← links)
- Phenylketonuria (Q39985) (← links)
- Classical phenylketonuria (Q39986) (← links)
- Embryofetopathy due to maternal phenylketonuria (Q39987) (← links)
- Nonclassical phenylketonuria (Q39988) (← links)
- Disorders of tyrosine metabolism (Q39989) (← links)
- Alkaptonuria (Q39990) (← links)
- Tyrosinaemia type 1 (Q39991) (← links)
- Tyrosinaemia type 2 (Q39992) (← links)
- Albinism or other specified genetically-determined hypomelanotic disorders (Q39993) (← links)
- Oculocutaneous albinism (Q39994) (← links)
- Disorders of histidine metabolism (Q39995) (← links)
- Histidinaemia (Q39996) (← links)
- Disorders of tryptophan metabolism (Q39997) (← links)
- Urocanic aciduria (Q39998) (← links)
- Carnosinaemia (Q39999) (← links)
- Maple-syrup-urine disease (Q40000) (← links)
- Classical organic aciduria (Q40001) (← links)
- Organic aciduria (Q40002) (← links)
- Cerebral organic aciduria (Q40003) (← links)
- Disorders of branched-chain amino acid metabolism (Q40004) (← links)
- Disorders of ketone body metabolism (Q40005) (← links)
- Inborn errors of fatty acid oxidation or ketone body metabolism (Q40006) (← links)
- Sjögren-Larsson syndrome (Q40007) (← links)
- Disorders of carnitine transport or the carnitine cycle (Q40008) (← links)
- Disorders of mitochondrial fatty acid oxidation (Q40009) (← links)
