Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to

Nume		Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Disorders of urea cycle metabolism

Boli A-Z		3-Hydroxyacyl-Coa Dehydrogenase Deficiency 3-Methylglutaconic Aciduria Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amino Acid Metabolic Disorder Aniridia 1 Anorexia Nervosa 1 Argininemia Argininosuccinic Aciduria Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Blood Group--Ahonen Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to Citrullinemia, Classic Cleft Palate, Isolated Eating Reflex Epilepsy Encephalopathy Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Learning Disability Ocular Motor Apraxia Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Orotic Aciduria Pancreatitis, Hereditary Postpartum Psychosis Propionic Acidemia Reye Syndrome Thoracic Outlet Syndrome Urea Cycle Disorder