Because of a lapse in government funding, the information on this website may not be up to date, transactions submitted via the website may not be processed, and the agency may not be able to respond to inquiries until appropriations are enacted. The NIH Clinical Center (the research hospital of NIH) is open. For more details about its operating status, please visit cc.nih.gov. Updates regarding government operating status and resumption of normal operations can be found at opm.gov.

NLM Logo

Homozygous Familial Hypercholesterolemia MeSH Descriptor Data 2026


MeSH Heading
Homozygous Familial Hypercholesterolemia
Tree Number(s)
C16.320.565.398.481.500
C18.452.584.500.500.644.475.500
C18.452.584.563.481.500
C18.452.648.398.481.500
Unique ID
D000090542
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000090542
Scope Note
A rare inherited genetic disorder, one form of HYPERLIPOPROTEINEMIA TYPE II, characterized by high level of LOW-DENSITY LIPOPROTEIN (LDL) which if not treated could elevate the chance of heart attack at an early age.
Entry Term(s)
HoFH
Previous Indexing
Hypercholesterolemia (1966-2021) / Hyperlipidemia/familial & genetic (1966-2021)
See Also
Receptors, LDL
Public MeSH Note
2022
History Note
2022
Date Introduced
2022/01/01
Last Updated
2022/04/13
Homozygous Familial Hypercholesterolemia Preferred
page delivered in 0.101s