Categorias DeCS
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.687 Phenylketonurias .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.766 Phenylketonurias .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.687 Phenylketonurias .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.687 Phenylketonurias .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.766 Phenylketonurias .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.687 Phenylketonurias .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.682 Oxidoreductases .
D08.811.682.660 Oxidoreductases Acting on CH-CH Group Donors .
D08.811.682.660.275 Dihydrodipicolinate Reductase .
D08.811.682.662 Oxidoreductases Acting on CH-NH Group Donors .
D08.811.682.662.582 Oxidoreductases, N-Demethylating .
D08.811.682.662.582.361 Dihydropteridine Reductase .
D08.811.682.662.825 Tetrahydrofolate Dehydrogenase .
D27 Chemical Actions and Uses .
D27.505 Pharmacologic Actions .
D27.505.519 Molecular Mechanisms of Pharmacological Action .
D27.505.519.389 Enzyme Inhibitors .
D27.505.519.389.350 Folic Acid Antagonists .
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Sinônimos e Históricos | Documentos
LILACS e MDL | | | | | | | | | | | | | | |
| Phenylketonurias .
BH4 Deficiency .
DHPR Deficiency .
Deficiency Disease, Dihydropteridine Reductase .
Deficiency Disease, Phenylalanine Hydroxylase .
Deficiency Disease, Phenylalanine Hydroxylase, Severe .
Dihydropteridine Reductase Deficiency .
Folling Disease .
Folling's Disease .
HPABH4C .
Hyperphenylalaninaemia .
Hyperphenylalaninemia Caused by a Defect in Biopterin Metabolism .
Hyperphenylalaninemia, BH4-Deficient, C .
Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due To DHPR Deficiency .
Non-Phenylketonuric Hyperphenylalaninemia .
Oligophrenia Phenylpyruvica .
PAH Deficiency .
PKU, Atypical .
Phenylalanine Hydroxylase Deficiency .
Phenylalanine Hydroxylase Deficiency Disease, Severe .
Phenylketonuria .
Phenylketonuria I .
Phenylketonuria II .
Phenylketonuria Type 2 .
Phenylketonuria, Atypical .
Phenylketonuria, Classical .
QDPR Deficiency .
Quinoid Dihydropteridine Reductase Deficiency .
Tetrahydrobiopterin Deficiency .
Atypical PKU .
Atypical Phenylketonuria .
Classical Phenylketonuria .
Deficiency, BH4 .
Deficiency, DHPR .
Deficiency, Dihydropteridine Reductase .
Deficiency, PAH .
Deficiency, Phenylalanine Hydroxylase .
Deficiency, QDPR .
Deficiency, Tetrahydrobiopterin .
Disease, Folling .
Disease, Folling's .
Hyperphenylalaninemia, Non Phenylketonuric .
Non Phenylketonuric Hyperphenylalaninemia .
Non-Phenylketonuric Hyperphenylalaninemias .
Dihydropteridine Reductase Deficiency Disease .
Hyperphenylalaninemia, Non-Phenylketonuric .
Phenylalanine Hydroxylase Deficiency Disease .
PHENYLKETONURIA .
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