Phenylalanine in the b phenylketonurias. Medical search. Frequent questions

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Organisms1

Anabaena variabilis

Diseases8

Phenylketonurias Phenylketonuria, Maternal Metabolism, Inborn Errors Microcephaly Congenital Hypothyroidism Intellectual Disability Amino Acid Metabolism, Inborn Errors Galactosemias

Chemicals and Drugs11

Phenylalanine Phenylalanine Hydroxylase Phenylalanine Ammonia-Lyase Phenylpyruvic Acids Biopterin Tyrosine Homogentisic Acid Amino Acids Fenclonine Pterins Phenylacetates

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Neonatal Screening Diet Therapy Diet, Protein-Restricted

Psychiatry and Psychology2

Intelligence Intellectual Disability

Phenomena and Processes1

Diet, Protein-Restricted

Named Groups1

Infant, Newborn

Health Care1

Neonatal Screening

Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Named Groups Health Care

Phenylketonurias Phenylalanine Phenylalanine Hydroxylase Phenylketonuria, Maternal Phenylalanine Ammonia-Lyase Phenylpyruvic Acids Biopterin Anabaena variabilis Neonatal Screening Tyrosine Metabolism, Inborn Errors Microcephaly Infant, Newborn Homogentisic Acid Amino Acids Intelligence Fenclonine Diet Therapy Congenital Hypothyroidism Intellectual Disability Diet, Protein-Restricted Pterins Amino Acid Metabolism, Inborn Errors Phenylacetates Galactosemias

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