MeSH Browser

MeSH Heading: Hypobetalipoproteinemia, Familial, Apolipoprotein B
Tree Number(s): C18.452.584.500.875.440.750; C18.452.584.563.497
Unique ID: D052476
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D052476
Scope Note: 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.
Entry Term(s): Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type; Apolipoprotein B Deficiency; Apolipoprotein B Deficiency Disease; Hypobetalipoproteinemia, Familial, Apo B
Previous Indexing: Apolipoproteins B (1986-2006)
Public MeSH Note: 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE see ABETALIPOPROTEINEMIA 2000-2006
History Note: 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE use ABETALIPOPROTEINEMIA 2000-2006
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2021/07/01

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

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psychology (PX)

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surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Hypobetalipoproteinemia, Familial, Apolipoprotein B MeSH Descriptor Data 2025