Informaţii despre

Nume Phenylketonuria
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Classical phenylketonuria; Other hyperphenylalaninaemias
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of Aging Agoraphobia Alacrima, Achalasia, and Mental Retardation Syndrome Alkaptonuria Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amino Acid Metabolic Disorder Aminoacidopathies Aminoaciduria Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Aortopulmonary Window Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Attention Deficit-Hyperactivity Disorder Autism Autoimmune Polyendocrine Syndrome Type 1 Band Heterotopia Biotinidase Deficiency Blau Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Breath-Holding Spells Central Precocious Puberty Cerebral Atrophy Cerebritis Cholestasis-Lymphedema Syndrome Citrullinemia, Type Ii, Neonatal-Onset Classic Phenylketonuria Cleft Larynx, Posterior Cognitive Function 1, Social Congenital Hypothyroidism Cortical Blindness Crouzon Syndrome with Acanthosis Nigricans Cystic Fibrosis Cystinuria Delusional Disorder Dementia Dyslexia Eosinophilia-Myalgia Syndrome Epilepsy Esophageal Atresia Fabry Disease Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fetal Alcohol Syndrome Focal Segmental Glomerulosclerosis Galactosemia Glycogen Storage Disease Hair Whorl Helicobacter Pylori Infection Hepatic Adenomas, Familial Hepatitis Hereditary Dystonia Hersh Podruch Weisskopk Syndrome Holoprosencephaly Homocystinuria Hyperglycinuria Hyperphenylalaninemia Hyperphenylalaninemia, Bh4-Deficient, B Hyperphenylalaninemia, Bh4-Deficient, C Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hypomelanotic Disorder Hypophosphatasia Inherited Metabolic Disorder Ischemia Keratomalacia Lesch-Nyhan Syndrome Leukemia Lissencephaly 1 Lobar Holoprosencephaly Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lymphoblastic Leukemia Maple Syrup Urine Disease Maternal Hyperphenylalaninemia Mevalonic Aciduria Microcephaly Mild Hyperphenylalaninemia Mild Phenylketonuria Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Carboxylase Deficiency Myotonia Congenita, Autosomal Dominant Neonatal Hypothyroidism Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Norse Nutritional Deficiency Disease Papillon-Lefevre Syndrome Paraplegia Partial Hydatidiform Mole Pemphigus Pemphigus Foliaceus Precocious Puberty Prosopagnosia Pulmonary Hypertension, Primary, 1 Pyloric Stenosis Pyruvate Kinase Deficiency of Red Cells Reye Syndrome Rickets Sandhoff Disease Segawa Syndrome, Autosomal Recessive Spasticity Spastic Paraparesis Succinyl-Coa:3-Oxoacid-Coa Transferase Deficiency Systemic Scleroderma Tay-Sachs Disease Tetraamelia Syndrome, Autosomal Recessive Tetrahydrobiopterin Deficiency Toxic Encephalopathy Tremor Tyrosinemia Tyrosinosis Undifferentiated Pleomorphic Sarcoma Vitamin B12 Deficiency West Syndrome