Hypoalphalipoproteinemias [hypoalfalipoproteinemie]
- Terms
-
familiární hypoalfalipoproteinemie
hypoalfalipoproteinémie
hypoalfalipoproteinémie familiární
-
alpha-Lipoprotein Deficiency Disease, Familial
Familial alpha-Lipoprotein Deficiency Disease
Familial High Density Lipoprotein Deficiency Disease
Familial High-Density Lipoprotein Deficiency Disease
HDL Cholesterol, Low Serum
HDL Lipoprotein Deficiency Disease
High-Density Lipoprotein Deficiency Disease, Familial
Hypo alpha Lipoproteinemia
Hypoalphalipoproteinemia
Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Primary
Lipoprotein Deficiency Disease, HDL, Familial
Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS.
- DUI
- D052456 MeSH Browser
- CUI
- M0487118
- Previous indexing
- Lipoproteins, HDL (1981-2006)
- History note
- 2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL use TANGIER DISEASE 1995-2006
- Public note
- 2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL see TANGIER DISEASE 1995-2006
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
Hdl Deficiency, Type 2 Disease MeSH Browser