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Deficiency Disease, Dihydropteridine Reductase, Deficiency Disease, Phenylalanine Hydroxylase, Deficiency Disease, Phenylalanine Hydroxylase, Severe, Dihydropteridine Reductase Deficiency Disease, Folling's Disease, Fölling's disease, Folling Disease, Hyperphenylalaninaemia, Hyperphenylalaninemia, Non-Phenylketonuric, Phenylalanine Hydroxylase Deficiency Disease, Phenylalanine Hydroxylase Deficiency Disease, Severe, Phenylketonuria, Phenylketonuria, Atypical, Phenylketonuria, Classical, Phenylketonuria I, Phenylketonuria II, Phenylketonurias — Déficit en dihydroptéridine réductase, Déficit en phénylalanine hydroxylase, Hyperphénylalaninémie, Hyperphénylalaninémie liée au déficit en dihydroptéridine réductase, Hyperphénylalaninémie non phénylcétonurique, Maladie de Fölling, Phénylcétonurie, Phénylcétonurie atypique, Phénylcétonurie classique, Phénylcétonurie de type 1, Phénylcétonurie de type 2, Phénylcétonuries - Maternal Phenylalanine Hydroxylase Deficiency Disease, Maternal Phenylketonuria, Phenylalanine-Hydroxylase Deficiency Disease, Maternal, Phenylketonuria, Maternal, PKU, Maternal, Pregnancy in Phenylketonuria — Déficit maternel en phénylalanine hydroxylase, Hyperphénylalaninémie maternelle, PCU maternelle, Phénylcétonurie maternelle[Analogie]
D08.811.682.690.708.601 • Phenylalaninase (n.) • Phenylalanine 4-hydroxylase (n.) • Phenylalanine 4-Hydroxylase (n.) • Phenylalanine 4-monooxygenase (n.) • Phenylalanine 4-Monooxygenase (n.) • Phenylalanine Hydroxylase (n.)
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