Inborn errors of metabolism like phenylketonuria. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Organisms1

Anabaena variabilis

Diseases17

Phenylketonurias Metabolism, Inborn Errors Phenylketonuria, Maternal Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Microcephaly Carbohydrate Metabolism, Inborn Errors Intellectual Disability Maple Syrup Urine Disease Urea Cycle Disorders, Inborn Brain Diseases, Metabolic, Inborn Congenital Hypothyroidism Argininosuccinic Aciduria Hyperammonemia Galactosemias

Chemicals and Drugs7

Phenylalanine Hydroxylase Phenylalanine Phenylpyruvic Acids Biopterin Phenylalanine Ammonia-Lyase Homogentisic Acid Tyrosine

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Neonatal Screening Diet, Protein-Restricted Diet Therapy

Psychiatry and Psychology2

Intellectual Disability Intelligence

Phenomena and Processes4

Diet, Protein-Restricted Mutation Energy Metabolism Lipid Metabolism

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 Metabolism, Inborn Errors Phenylketonuria, Maternal Phenylalanine Hydroxylase Phenylalanine Amino Acid Metabolism, Inborn Errors Neonatal Screening Phenylpyruvic Acids Biopterin Anabaena variabilis Infant, Newborn Lipid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Microcephaly Carbohydrate Metabolism, Inborn Errors Intellectual Disability Diet, Protein-Restricted Maple Syrup Urine Disease Urea Cycle Disorders, Inborn Diet Therapy Intelligence Phenylalanine Ammonia-Lyase Homogentisic Acid Brain Diseases, Metabolic, Inborn Mutation Congenital Hypothyroidism Argininosuccinic Aciduria Hyperammonemia Energy Metabolism Tyrosine Lipid Metabolism Galactosemias

No FAQ available that match "inborn errors of metabolism like phenylketonuria"