Informaţii despre

Nume Citrullinemia, Classic
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Disorders of urea cycle metabolism

Vezi şi

Boli A-Z Acute Neonatal Citrullinemia Type I Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amino Acid Metabolic Disorder Aniridia 1 Anorexia Nervosa 1 Argininemia Argininosuccinic Aciduria Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Autosomal Recessive Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to Citrullinemia, Type Ii, Adult-Onset Citrullinemia, Type Ii, Neonatal-Onset Collecting Duct Carcinoma Duodenitis Encephalitis Encephalopathy Epilepsy Fatty Liver Disease Hepatitis Hepatocellular Carcinoma Hyperlysinemia, Type I Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome Hypertrophic Pyloric Stenosis Immune Suppression Liver Cirrhosis Liver Disease Lysinuric Protein Intolerance Maple Syrup Urine Disease Neurodegeneration with Brain Iron Accumulation 2a Neutropenia Nonalcoholic Steatohepatitis Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Orotic Aciduria Pancreatitis Papilledema Pili Torti Postpartum Psychosis Propionic Acidemia Pyloric Stenosis Pyruvate Carboxylase Deficiency Reye Syndrome Schizophrenia Somatostatinoma Status Epilepticus Transposition of the Great Arteries Undifferentiated Pleomorphic Sarcoma Urea Cycle Disorder