-
Hypoalphalipoproteinemia is a high-density
lipoprotein deficiency,
inherited in an
autosomal dominant manner. It can be ****ociated with LDL receptor. ****ociated...
-
Tangier disease or
hypoalphalipoproteinemia is an
extremely rare
inherited disorder characterized by a
severe reduction in the
amount of high
density lipoprotein...
-
lipoproteins in the blood. It
occurs in
genetic disorders (e.g.
hypoalphalipoproteinemia, hypobetalipoproteinemia), malnutrition, malabsorption, wasting...
- Y,
Yamamoto N, et al. (February 1999). "Frequent
occurrence of
hypoalphalipoproteinemia due to
mutant apolipoprotein A-I gene in the po****tion: a po****tion-based...
- Hyperoxaluria,
primary AGXT, GRHPR,
DHDPSL Hyperphenylalaninemia 12q
Hypoalphalipoproteinemia (Tangier disease) ABCA1
Hypochondrogenesis COL2A1 Hypochondroplasia...
-
Abetalipoproteinemia B****en-Kornzweig
syndrome High-density
lipoid deficiency Hypoalphalipoproteinemia Hypobetalipoproteinemia (familial) 272.6
Lipodystrophy 272.7 Lipidoses...
- 2022-03-16.
Retrieved 2024-03-11. "CER-001 for
Familial Primary Hypoalphalipoproteinemia". NIHR
Innovation Observatory Evidence Briefing. May 2018. Archived...
- Hypoaldosteronism, congenital, due to CMO II deficiency; 610600; CYP11B2
Hypoalphalipoproteinemia; 604091; APOA1 Hypocalcemia,
autosomal dominant; 146200; CASR Hypocalciuric...
