Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to

Nume		Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Disorders of ornithine metabolism
Clasificare anatomică Malacards		Boli neuronale

Boli A-Z		Acute Pancreatitis Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alkaptonuria 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 Attention Deficit-Hyperactivity Disorder Beta-Ureidopropionase Deficiency Blood Group--Ahonen Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to Cat Eye Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Citrullinemia, Classic Citrullinemia, Type Ii, Adult-Onset Encephalopathy Headache Hepatic Adenomas, Familial Hepatitis Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Lysinuric Protein Intolerance Neuroblastoma Ocular Motor Apraxia Orotic Aciduria Pancreatitis Postpartum Psychosis Propionic Acidemia Pyrimidine Metabolic Disorder Reye Syndrome Subacute Delirium Thoracic Outlet Syndrome Urea Cycle Disorder