Linked from

The 12 pages that link to Phenylketonuria, each with the reason it gives.

• Amino acidRelated: It shows how failure to metabolize one amino acid can damage the nervous system.

• Newborn screeningBroader topic: Its early detection and treatment helped establish the value of newborn screening.

• PhenotypeBroader topic: Dietary treatment can prevent much of its otherwise severe phenotype.

• Essential amino acidCompared with: It shows that dietary amino acid needs can also be constrained by metabolic disease.

• TyrosineRelated: Low conversion of phenylalanine to tyrosine makes dietary tyrosine important in its management.

• Genotype–phenotype correlationBroader topic: Its severity depends strongly on both PAH variants and dietary phenylalanine exposure.

• AspartameRelated: People with phenylketonuria must restrict phenylalanine, so aspartame products carry warnings.

• PhenylalanineBroader topic: This disorder makes controlling phenylalanine intake medically essential.

• Maple syrup urine diseaseCompared with: Both disorders require dietary amino-acid management, but they affect different amino acids and pathways.

• Metabolic disorderBroader topic: It illustrates how early dietary treatment can prevent severe consequences of a metabolic defect.

• Recessive traitBroader topic: Its usual inheritance pattern is autosomal recessive.

• Nutritional and Metabolic DiseasesBroader topic: It shows how a single inherited metabolic defect can make dietary management essential.