Informaţii despre

Nume Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Other specified disorders of carbohydrate metabolism

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Boli A-Z Acute Insulin Response Acute Liver Failure Acute Lymphocytic Leukemia Acute Pancreatitis Alcohol Abuse Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amblyopia Aniridia 1 Anorexia Nervosa 1 Argininemia Argininosuccinic Aciduria Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Blood Group--Ahonen Blood Group, I System Brain Edema Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to Carbonic Anhydrase Va Deficiency Cat Eye Syndrome Cerebritis Childhood Apraxia of Speech Citrullinemia, Classic Citrullinemia, Type Ii, Neonatal-Onset Colorectal Cancer Congenital Extrahepatic Portosystemic Shunt Congenital Portosystemic Shunt Encephalomalacia Encephalopathy Fasting Hypoglycemia Gastric Cancer Glucose Transporter Type 1 Deficiency Syndrome Gyrate Atrophy of Choroid and Retina Hemoglobinuria Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatocellular Carcinoma Herpes Simplex Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperinsulinism Hyperlysinuria with Hyperammonemia Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypoglycemia Hypopituitarism Influenza Intracranial Hypertension Isovaleric Acidemia Lactic Acidosis Leukemia Leukodystrophy Liver Cirrhosis Liver Disease Lymphoblastic Leukemia Lysinuric Protein Intolerance Metabolic Acidosis Mucopolysaccharidosis-Plus Syndrome N-Acetylglutamate Synthase Deficiency Neonatal Herpes Ocular Motor Apraxia Organic Acidemia Ornithinemia Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Orotic Aciduria Pancreatitis Papillomatosis, Confluent and Reticulated Paroxysmal Nocturnal Hemoglobinuria Portal Hypertension Postpartum Psychosis Propionic Acidemia Pulmonary Arteriovenous Malformation Pyruvate Carboxylase Deficiency Renal Tubular Acidosis Reye Syndrome Seizure Disorder Silver-Russell Syndrome Status Epilepticus Thoracic Outlet Syndrome Urea Cycle Disorder Ureterocele Urethritis Visceral Steatosis Weber Syndrome