MeSH Browser

MeSH Supplementary: apolipoprotein E2 (Bethesda)
Unique ID: C038969
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C038969
Entry Term(s): apo E-Bethesda; apo E2 (Bethesda); apo-E-Bethesda; apolipoprotein E-Bethesda
Registry Numbers: 0
Previous Indexing: *APOLIPOPROTEINS (83-84)
Heading Mapped to: *Apolipoprotein E2
Frequency: 2
Note: a variant of apolipoprotein E2 isoform; derived from a mutation of the E2 or E2* allele; associated with type III hyperlipoproteinemia
Source: J Clin Endocrinol Metab 1983;57(5):969
Date of Entry: 1983/10/28
Revision Date: 2006/08/04

Concept UI: M0116958
Registry Numbers: 0
Terms: apolipoprotein E2 (Bethesda) Preferred Term
Term UI T661817
Date12/08/2005
LexicalTag NON
ThesaurusID NLM (2005); apo E-Bethesda
Term UI T146960
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1983); apo E2 (Bethesda)
Term UI T661832
Date12/08/2005
LexicalTag NON
ThesaurusID NLM (2005); apo-E-Bethesda
Term UI T146961
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1983); apolipoprotein E-Bethesda
Term UI T146962
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1983)

apolipoprotein E2 (Bethesda) MeSH Supplementary Concept Data 2025