• Thumbnail for Hyperprolinemia
    Hyperprolinemia is a condition which occurs when the amino acid proline is not broken down properly by the enzymes proline oxidase or pyrroline-5-carboxylate...
    8 KB (784 words) - 17:55, 28 October 2024
  • Thumbnail for Asymptomatic
    pressure) Histidinemia HIV (AIDS) HPV Hyperaldosteronism hyperlipidaemia Hyperprolinemia type I Hypothyroidism Hypoxia (some cases) Idiopathic thrombocytopenic...
    8 KB (846 words) - 03:16, 12 November 2024
  • proline can be synthesized from diethyl malonate and acrylonitrile: Hyperprolinemia Inborn error of metabolism Prolidase deficiency Prolinol "Proline"...
    23 KB (2,240 words) - 05:28, 11 November 2024
  • Hyperphenylalaninemic embryopathy Hyperpipecolatemia Hyperprolactinemia Hyperprolinemia type II Hyperprolinemia Hyperreflexia Hyper-reninism Hypersensitivity Hypersensitivity...
    21 KB (1,717 words) - 04:04, 12 March 2024
  • Thumbnail for Congenital disorders of amino acid metabolism
    Hypermethioninemia Hyperlysinemias Nonketotic hyperglycinemia Propionic acidemia Hyperprolinemia Cystinuria Dicarboxylic aminoaciduria Hartnup disease Glutaric acidemia...
    2 KB (71 words) - 15:18, 10 November 2024
  • Thumbnail for Aldehyde dehydrogenase 4 family, member A1
    to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of...
    5 KB (675 words) - 11:37, 15 November 2024
  • Thumbnail for Proline oxidase
    catabolism. Deletion of this gene has been associated with type I hyperprolinemia. The gene is located on chromosome 22q11.21, a region which has also...
    12 KB (1,549 words) - 12:01, 24 December 2023
  • Thumbnail for Glutamate receptor
    Hydroxybutyric aminoaciduria Hyperhomocysteinemia and homocysteinuria Hyperprolinemia Lead encephalopathy Leber's disease MELAS syndrome MERRF Mitochondrial...
    63 KB (6,876 words) - 07:52, 2 November 2024
  • Thumbnail for Proline dehydrogenase
    on the chromosomes 22 and 19, respectively. Their mutations lead to hyperprolinemia, manifested by increased proline levels in blood and urine. The deficiency...
    7 KB (771 words) - 00:41, 28 November 2023
  • Thumbnail for Carnosinemia
    indicator, is the underlying metabolic cause of carnosinemia. Histidinemia Hyperprolinemia Inborn errors of metabolism Proline Online Mendelian Inheritance in...
    10 KB (1,061 words) - 15:33, 16 October 2024
  • Hyperpigmentation, familial progressive; 145250; KITLG Hyperprolinemia, type I; 239500; PRODH Hyperprolinemia, type II; 239510; ALDH4A1 Hypertension, early-onset...
    234 KB (18,877 words) - 06:16, 6 November 2024