Terminology Service for NFDI4Health
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hyperalphalipoproteinemia

Go to external page http://purl.obolibrary.org/obo/MONDO_0015903

An autosomal dominant genetic condition caused by mutation(s) in the CETP gene, encoding cholesteryl ester transfer protein. Affected individuals may have increased longevity due to decreased risk of coronary heart disease. [ ]

Term info

Label

hyperalphalipoproteinemia

Synonyms
  • HALP1
database cross reference
Subsets

disease_grouping, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/NCIT_C128806, http://linkedlifedata.com/resource/umls/id/C0342883, http://purl.obolibrary.org/obo/Orphanet_181428, http://identifiers.org/snomedct/238080004

id

MONDO:0015903

narrowMatch

https://icd.codes/icd10cm/E78.4

Term relations