Pages that link to "Phenylketonuria"
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The following pages link to Phenylketonuria:
Displayed 204 items.
- Tyrosinemia (← links)
- Hyperreflexia (← links)
- Pulmonary valve stenosis (← links)
- Ddx:Epilepsy (← links)
- Pallor (← links)
- Hypomelanosis (← links)
- Intrauterine growth retardation (← links)
- Trimethylaminuria (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- PKU (redirect page) (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- List of genetic disorders (← links)
- List of genetic engineering topics (← links)
- List of geneticists (← links)
- Tetrahydrobiopterin (← links)
- Testpage3 (← links)
- Tetralogy of fallot overview (← links)
- Tetralogy of fallot causes (← links)
- Sapropterin (← links)
- The Myelin Project (← links)
- ICD-10 Chapter E (← links)
- Autosomal recessive (← links)
- List of medical abbreviations (← links)
- List of diseases (P) (← links)
- List of genetic disorders (← links)
- Cholesteryl ester storage disease (← links)
- Newborn screening (← links)
- Batten disease (← links)
- Bowen's disease (← links)
- Dopaminergic (← links)
- Zolmitriptan (oral) (← links)
- Chromosome 12 (human) (← links)
- List of genetics-related topics (← links)
- Pleiotropy (← links)
- Genetics (← links)
- Dominance relationship (← links)
- Allele (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Glucose-galactose malabsorption (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hyperlysinemia (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- N-Acetylglutamate synthase deficiency (← links)
- Ornithine transcarbamylase deficiency (← links)
- Ornithine translocase deficiency (← links)
- Prolidase deficiency (← links)
- Pyruvate carboxylase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Tetrahydrobiopterin deficiency (← links)
- Urea cycle disorder (← links)
- Variegate porphyria (← links)
- List of genetic engineering topics (← links)
- Phenylalanine hydroxylase (← links)
- GTP cyclohydrolase I (← links)
- Peter Tishler (← links)
- List of geneticists (← links)
- Nutritional genomics (← links)
- Public Health Genomics (← links)
- Mixed disorder of acid-base balance (← links)
- Phenylalanine racemase (ATP-hydrolysing) (← links)
- Inborn error of metabolism (← links)
- Enzyme (← links)
- Causes of hypoglycemia (← links)
- Disorders of calcium metabolism (← links)
- Amino acid (← links)
- Essential amino acid (← links)
- Reductive acetyl CoA Pathway (← links)
- Entner-Doudoroff Pathway (← links)
- Wikipedia:Wikiproject Metabolic Pathways/templates (← links)
- Glucose-6-phosphate (← links)
- Teratology (← links)
- Fetal alcohol syndrome (← links)
- Phenylalanine (← links)
- Tetrahydrobiopterin (← links)
- List of fatty acid metabolism disorders (← links)
- Atazanavir (← links)
- Chlorpromazine (oral) (← links)
- Mesalamine (oral) (← links)
- Mycophenolate (← links)
- Alitame (← links)
- Aspartame (← links)
- Raltegravir (← links)
- Trifluoperazine (← links)
- Tourettism (← links)
- Gangliosidosis (← links)
- Growth failure (← links)
- Renal glycosuria (← links)
- Testpage3 (← links)
- Sialidosis (← links)
- List of amino acid metabolism disorders (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Pseudo-Hurler polydystrophy (← links)
- Hepatoerythropoietic porphyria (← links)
- Hyperactivity (← links)
- Recessive gene (← links)
- Classical Phenylketonuria (redirect page) (← links)
- Deficiency disease, Phenylalanine Hydroxylase (redirect page) (← links)
- Folling disease (redirect page) (← links)
- Hyperphenylalaninemia (redirect page) (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- List of genetic disorders (← links)
- Dopaminergic (← links)
- 6-Pyruvoyltetrahydropterin synthase deficiency (← links)
- Phenylalanine hydroxylase (← links)
- GTP cyclohydrolase I (← links)
- Biopterin (← links)
- Pyrimethamine (← links)
- Testpage3 (← links)
- Guthrie test (← links)
- PCBD1 (← links)
- Pyrimethamine adverse reactions (← links)
- Sapropterin (← links)
- Aspartylglucosaminuria (← links)
- Cystathioninuria (← links)
- Type I and type II errors (← links)
- List of psychology topics (← links)
- Aspartame controversy (← links)
- Genetic testing (← links)
- Xeroderma (← links)
- Guthrie test (← links)
- Neonatal heel prick (← links)
- ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Chromosome 12 (← links)
- Small for gestational age (← links)
- The Living Textbook of Endocrinology (← links)
- The Living Textbook of Metabolic disorders (← links)
- The WikiDoc Living Textbook of Endocrinology (← links)
- The WikiDoc Living Textbook of Metabolic Disorders (← links)
- Autism epidemiology (← links)
- Spasticity (← links)
- Rhesus Macaque (← links)
- ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases (← links)
- Nature versus nurture (← links)
- GSTZ1 (← links)
- Dihydrobiopterin reductase (← links)
- Inborn errors of renal tubular transport (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Phenylketonuric (← links)
- Hawkinsinuria (← links)
- Inborn errors of amino acid metabolism (← links)
- D-Glyceric acidemia (← links)
- Urocanic aciduria (← links)
- Amino acid transport disorder (← links)
- Argininemia (← links)
- 2-Hydroxyglutaric aciduria (← links)
- Type I tyrosinemia (← links)
- Type II tyrosinemia (← links)
- Type III tyrosinemia (← links)
- WikiPatient: Metabolic Disease (← links)
- Congenital heart disease causes (← links)
- Tetralogy of fallot overview (← links)
- Tetralogy of fallot causes (← links)
- Tricuspid atresia overview (← links)
- Phenylketonuria (patient information) (← links)
- Patent ductus arteriosus primary prevention (← links)
- Urine odor (← links)
- Uncontrolled phenylketonuria in the mother (redirect to section "Maternal phenylketonuria") (← links)
- Mental retardation medical therapy (← links)
- Seizure causes (← links)
- Autism pathophysiology (← links)
- Microcephaly causes (← links)
- Tricuspid atresia risk factors (← links)
- Epilepsy causes (← links)
- Hyperhidrosis causes (← links)
- Disequilibrium causes (← links)
- WBR0087 (← links)
- WBR0302 (← links)
- WBR0255 (← links)
- Phenylketonurics (redirect page) (← links)
- Sugar substitute (← links)
- Lacosamide (← links)
- Sapropterin (← links)
- Prochlorperazine (injection) (← links)
- Phenylketonuria overview (← links)
- Phenylketonuria historical perspective (← links)
- Phenylketonuria pathophysiology (← links)
- Phenylketonuria classification (← links)
- Phenylketonuria causes (← links)
- Phenylketonuria differential diagnosis (← links)
- Phenylketonuria epidemiology and demographics (← links)
- Phenylketonuria risk factors (← links)
- Phenylketonuria natural history, complications and prognosis (← links)
- Phenylketonuria screening (← links)
- Phenylketonuria history and symptoms (← links)
- Phenylketonuria physical examination (← links)
- Phenylketonuria laboratory findings (← links)
- Phenylketonuria other diagnostic studies (← links)
- Phenylketonuria medical therapy (← links)
- Phenylketonuria secondary prevention (← links)
- Phenylketonuria primary prevention (← links)
- Phenylketonuria cost-effectiveness of therapy (← links)
- Phenylketonuria future or investigational therapies (← links)
- Phenylketonuria case study one (← links)
- Classic PKU (redirect page) (← links)
- Classic phenylketonuria (redirect page) (← links)
- Mild phenylketonuria (redirect page) (← links)
- Maternal phenylketonuria (redirect page) (← links)
- Mild PKU (redirect page) (← links)
- Maternal PKU (redirect page) (← links)
- Classical PKU (redirect page) (← links)
- Classic Phenylketonuria (redirect page) (← links)
- Mild Phenylketonuria (redirect page) (← links)
- Classical phenylketonuria (redirect page) (← links)
- Maternal Phenylketonuria (redirect page) (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Phenylketonuria electrocardiogram (← links)
- Phenylketonuria MRI (← links)
- Phenylketonuria CT (← links)
- Phenylketonuria ultrasound (← links)
- Phenylketonuria x ray (← links)
- Phenylketonuria surgery (← links)
- Phenylketonuria other imaging findings (← links)
- Sandbox:Mental retardation causes (← links)
- Sandbox:Pulmonary valve stenosis (← links)
- Pegvaliase (← links)
- Template:Metabolic pathway (← links)
- Template:Metabolic pathology (← links)
- Template:Amino acid metabolic pathology (← links)
- Template:Phenylketonuria (← links)