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765 Possible Causes for Hartnup Disease

  • Tryptophanemia

    Keywords: Pellagroid rash, Aminoaciduria, Hartnup disease How to cite this article: Amladi T S, Kohli M. Hartnup disease.[ijdvl.com] disease, [5] a disorder of amino acid transport. [6] However, the increase of tryptophan in that disorder is negligible when compared to that of hypertryptophanemia. [1][en.wikipedia.org] disease, Hawkinsunuria, Histidinemia, Histidinuria, Homocystinuria, Hydroxylysinuria, Hyperammonemia Hyperornithinemia Homocitrullinuria Syndrome (HHH), Hyperglycinuria ([geno.ma]

  • Pellagra

    The disease may occur secondary to malnutrition or malabsorption; inborn errors of metabolism or transport, as in Hartnup disease; deviation of precursors of niacin, as in[ncbi.nlm.nih.gov] The laboratory findings were not typical of Hartnup disease: aminoaciduris and indicanuria were absent and there was no evidence of tryptophan malabsorption.[ncbi.nlm.nih.gov] On DermNet NZ: Malnutrition Other websites: Dermatologic Manifestations of Pellagra – Medscape Drugs & Diseases Hartnup Disease – Medscape Drugs & Diseases[dermnetnz.org]

  • Sarcosinemia

    A fourth child had sarcosinemia detected through family screening after his brother was found to have Hartnup disease by neonatal urine screening.[ncbi.nlm.nih.gov]

  • Hartnup Disease

    What causes Hartnup disease? Hartnup disease is an autosomal recessive disorder.[symptoma.com] […] defect Neutral 1 amino acid transport defect Hartnup disorder HND Hartnup Disease Aminoaciduria, Hartnup type HARTNUP DISORDER; HND edit English Hartnup disease Human disease[wikidata.org] Hartnup disease Other names Aminoaciduria, Hartnup type Tryptophan Specialty Endocrinology Hartnup disease has an autosomal recessive pattern of inheritance.[en.wikipedia.org]

  • Iminoglycinuria

    See Hartnup disease.[encyclo.co.uk] For other hereditary disorders of amino acid transport, see also cystinuria ; Hartnup disease ; de Toni-Fanconi syndrome ( de Toni–Fanconi syndrome ). * * * Universalium.[universalium.academic.ru] For other hereditary disorders of amino acid transport, see also cystinuria ; Hartnup disease ; de Toni-Fanconi syndrome.[britannica.com]

  • Velocardiofacial Syndrome

    Velocardiofacial syndrome is classically characterized by clefting of the secondary palate, cardiac defects, learning disabilities, and facial dysmorphism. Knowledge of this syndrome is of significant importance to otolaryngologists because a failure to recognize it prior to head and neck surgery can result in serious[…][ncbi.nlm.nih.gov]

  • Hyperdibasic Aminoaciduria Type 1

    Hartnup Disease An autosomal recessive disorder due to defective absorption of NEUTRAL AMINO ACIDS by both the intestine and the PROXIMAL RENAL TUBULES.[ncbi.nlm.nih.gov] disease Lysinuric protein intolerance Iminoglycinuria Fanconi syndrome : Oculocerebrorenal syndrome Cystinosis Other Trimethylaminuria 2-Hydroxyglutaric aciduria Fumarase[dictionary.sensagent.com] disease ) · SLC7A7 ( Lysinuric protein intolerance ) · SLC7A9 ( Cystinuria ) 11-20 SLC11A1 ( Crohn's disease ) · SLC12A3 ( Gitelman syndrome ) · SLC16A1 ( HHF7 ) · SLC16A2[dictionary.sensagent.com]

  • Disorder of Sulfur-Bearing Amino Acid Metabolism

    disease E72.03 Lowe's syndrome E72.04 Cystinosis E72.09 Other disorders of amino-acid transport E72.10 Disorders of sulfur-bearing amino-acid metabolism, unspecified E72.11[healthprovidersdata.com] disease E72.03 Lowe's syndrome E72.04 Cystinosis E72.09 Other disorders of amino-acid transport E72.1 Disorders of sulfur-bearing amino-acid metabolism E72.11 Homocystinuria[healthprovidersdata.com] .-) E72.0 Disorders of amino-acid transport E72.00 Disorders of amino-acid transport, unspecified E72.01 Cystinuria E72.02 Hartnup's disease E72.03 Lowe's syndrome E72.04[icd10coded.com]

  • Malabsorption Syndrome

    For other hereditary disorders of amino acid transport, see also cystinuria; Hartnup disease; de Toni-Fanconi syndrome. Read More[britannica.com] Inherited defects include glucose-galactose malabsorption, abetalipoproteinemia, cystinuria, and Hartnup disease.[emedicine.medscape.com] […] disease Learn about this topic in these articles: iminoglycinuria In iminoglycinuria …“blue diaper syndrome”), and the methionine malabsorption syndrome (or “oasthouse urine disease[britannica.com]

  • Lysinemia

    Hartnup disease m. Imino glycinuria n. Galactosemia o. Refsum disease p. Porphyria q. Wilson ?disease r.[jalananil.tripod.com] Nama Penyakit Gangguan  Hartnup s disease triptofan 44. BIOSINTESIS ASAM AMINO 45. BIOSINTESIS ASAM AMINO 46. PRODUK KHUSUS DARI ASAM AMINO[pt.slideshare.net] Hartnup disease,ハートナップ病 99% 3. dibasic amino aciduria,二塩基性アミノ酸尿症 95 99% 4. iminoglycinuria,イミノグリシン尿症 99% 5. secondary iminoglycinuria,二次性イミノグリシン尿症 95 99% 6. transient neonatal[jc-metabolomics.com]

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