Hypobetalipoproteinemia, Familial, Apolipoprotein B [familiární hypobetalipoproteinemie, apolipoprotein B]
- Terms
-
apolipoprotein B - nedostatek
hypobetalipoproteinémie familiární, apolipoprotein B
hypobetalipoproteinemie spojené s modifikovanými apo B
hypobetalipoproteinémie vrozená, apolipoprotein B
hypobetalipoproteinémie, normální triacylglycerolémie, Steinbergův typ
-
Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type
Apolipoprotein B Deficiency
Apolipoprotein B Deficiency Disease
Hypobetalipoproteinemia, Familial, Apo B
An autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.
- DUI
- D052476 MeSH Browser
- CUI
- M0487158
- Previous indexing
- Apolipoproteins B (1986-2006)
- History note
- 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE use ABETALIPOPROTEINEMIA 2000-2006
- Public note
- 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE see ABETALIPOPROTEINEMIA 2000-2006
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 1
- DI
- diagnosis 1
- 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 1
- UR
- urine
- VE
- veterinary
- VI
- virology
Hypobetalipoproteinemia, Familial, 1 Disease MeSH Browser