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There is a page named "Hypoalphalipoproteinemia" on Wikipedia

  • Thumbnail for Hypoalphalipoproteinemia
    Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner. It can be associated with LDL receptor. Associated...
    3 KB (128 words) - 14:50, 9 April 2024
  • Familial Hypoalphalipoproteinemia
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    Tangier disease or hypoalphalipoproteinemia is an extremely rare inherited disorder characterized by a severe reduction in the amount of high density lipoprotein...
    8 KB (875 words) - 18:40, 1 January 2024
  • lipoproteins in the blood. It occurs in genetic disorders (e.g. hypoalphalipoproteinemia, hypobetalipoproteinemia), malnutrition, malabsorption, wasting...
    4 KB (327 words) - 18:14, 19 December 2023
  • Hyperoxaluria, primary AGXT, GRHPR, DHDPSL Hyperphenylalaninemia 12q Hypoalphalipoproteinemia (Tangier disease) ABCA1 Hypochondrogenesis COL2A1 Hypochondroplasia...
    42 KB (969 words) - 16:02, 3 April 2024
  • Thumbnail for Apolipoprotein AI
    Y, Yamamoto N, et al. (February 1999). "Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-I gene in the population: a population-based...
    21 KB (2,555 words) - 16:59, 6 May 2024
  • 2022-03-16. Retrieved 2024-03-11. "CER-001 for Familial Primary Hypoalphalipoproteinemia". NIHR Innovation Observatory Evidence Briefing. May 2018. Archived...
    9 KB (720 words) - 08:01, 12 May 2024
  • Abetalipoproteinemia Bassen-Kornzweig syndrome High-density lipoid deficiency Hypoalphalipoproteinemia Hypobetalipoproteinemia (familial) 272.6 Lipodystrophy 272.7 Lipidoses...
    16 KB (1,399 words) - 17:41, 9 February 2024
  • Hypoaldosteronism, congenital, due to CMO II deficiency; 610600; CYP11B2 Hypoalphalipoproteinemia; 604091; APOA1 Hypocalcemia, autosomal dominant; 146200; CASR Hypocalciuric...
    234 KB (18,877 words) - 15:43, 9 May 2024