Search
Descriptor English: Hypobetalipoproteinemias
Descriptor Spanish: Hipobetalipoproteinemias
Descriptor hipobetalipoproteinemias
Entry term(s) hipobetalipoproteinemia
Scope note: Afecciones con concentraciones sanguíneas anormalmente bajas de BETALIPOPROTEÍNAS (lipoproteínas de baja densidad o LDL). La hipobetalipoproteinemia es definida por valores de LDL iguales o inferiores al percentil 5 de la población. La afección comprende la forma autosómica dominante producida por mutación del gen de las APOLIPOPROTEÍNAS B, la forma recesiva por mutación de la proteína microsómica de transferencia de triglicéridos. Todas las formas se caracterizan por concentraciones bajas de LDL y malabsorción de la grasa de la dieta.
Descriptor Portuguese: Hipobetalipoproteinemias
Descriptor French: Hypobêtalipoprotéinémies
Entry term(s): Familial Hypobetalipoproteinemia
Hypo beta Lipoproteinemia
Hypo beta Lipoproteinemias
Hypobetalipoproteinemia
Tree number(s): C16.320.565.398.500.440
C18.452.584.500.875.440
C18.452.584.563.500.440
C18.452.648.398.500.440
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D006995
Scope note: Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Blood Protein Disorders (1966-1977)
Lipid Metabolism, Inborn Errors (1966-1977)
Lipoproteins (1966-1977)
Lipoproteins, LDL (1972-1977)
Public MeSH Note: 2007; see HYPOBETALIPOPROTEINEMIA 1991-2006, see HYPOLIPOPROTEINEMIA 1980-1990, see HYPOLIPOPROTEINEMIAS 1978-1979
History Note: 2007 (1978)
DeCS ID: 7171
Unique ID: D006995
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1977/04/29
Revision Date: 2013/07/08
Hypobetalipoproteinemias - Preferred
Concept UI M0010890
Scope note Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption.
Preferred term Hypobetalipoproteinemias
Entry term(s) Familial Hypobetalipoproteinemia
Hypo beta Lipoproteinemia
Hypo beta Lipoproteinemias
Hypobetalipoproteinemia



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.

Go to survey