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Medical condition
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
Hyperprolinemia
Patient is a carrier for a disease or infection but experiences no symptoms
pressure) Histidinemia HIV (AIDS) HPV Hyperaldosteronism hyperlipidaemia Hyperprolinemia type I Hypothyroidism Hypoxia (some cases) Idiopathic thrombocytopenic
Asymptomatic
Chemical compound
proline can be synthesized from diethyl malonate and acrylonitrile: Hyperprolinemia Inborn error of metabolism Prolidase deficiency Prolinol "Proline"
Proline
Protein-coding gene in the species Homo sapiens
to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of
Aldehyde dehydrogenase 4 family, member A1
Aldehyde_dehydrogenase_4_family,_member_A1
Enzyme
on the chromosomes 22 and 19, respectively. Their mutations lead to hyperprolinemia, manifested by increased proline levels in blood and urine. The deficiency
Proline_dehydrogenase
Medical condition
Hypermethioninemia Hyperlysinemias Nonketotic hyperglycinemia Propionic acidemia Hyperprolinemia Cystinuria Dicarboxylic aminoaciduria Hartnup disease Glutaric acidemia
Congenital disorders of amino acid metabolism
Congenital_disorders_of_amino_acid_metabolism
Disease
patients and their families should seek genetic counseling. Histidinemia Hyperprolinemia Inborn errors of metabolism Proline Online Mendelian Inheritance in
Carnosinemia
Protein-coding gene in the species Homo sapiens
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
Proline_oxidase
Neuron membrane protein
Hydroxybutyric aminoaciduria Hyperhomocysteinemia and homocysteinuria Hyperprolinemia Lead encephalopathy Leber's disease MELAS syndrome MERRF Mitochondrial
Glutamate_receptor
Hyperphenylalaninemic embryopathy Hyperpipecolatemia Hyperprolactinemia Hyperprolinemia type II Hyperprolinemia Hyperreflexia Hyper-reninism Hypersensitivity Hypersensitivity
List_of_diseases_(H)
Hyperpigmentation, familial progressive; 145250; KITLG Hyperprolinemia, type I; 239500; PRODH Hyperprolinemia, type II; 239510; ALDH4A1 Hypertension, early-onset
List_of_OMIM_disorder_codes
HYPERPROLINEMIA
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HYPERPROLINEMIA
Boy/Male
Indian, Sanskrit
Descendant of Fire
Boy/Male
Arabic, Australian, German, Muslim, Turkish
Pleasure
Boy/Male
Indian
Servant of God
Surname or Lastname
English (chiefly West Midlands)
English (chiefly West Midlands) : metonymic occupational name for a fuller, from Middle English tred(en) ‘to tread’ + well ‘well’. Fulling was the process by which newly woven cloth was cleaned and shrunk by the use of heat, water, and pressure (from treading) before finally being stretched and laid out to dry on tenter hooks.
Girl/Female
Australian, British, Chinese, Christian, English, Jamaican, Portuguese
Compound of the Names Polly and Anna; Bitter; Gracious; One who Plays for Real Madrid
Surname or Lastname
English
English : variant of Hyslop.
Boy/Male
Tamil
Aparant | அபராநà¯à®¤
Clear
Boy/Male
Hindu, Indian
Nectar of Victory
Girl/Female
Arabic, Muslim
Beneficial; Advantagious; Useful; Good; Profitable
Boy/Male
French American Biblical English
Prosperous protector. A FrenchOld English name Eadmund, meaning rich or happy, and protection.
HYPERPROLINEMIA
HYPERPROLINEMIA
HYPERPROLINEMIA
HYPERPROLINEMIA
HYPERPROLINEMIA