You are using an outdated browser. Please upgrade your browser to improve your experience.
hyperalphalipoproteinemia
Disease Summary
Associated Targets (3)
Tchem
2
Tclin
1
Mondo Description 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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
NCIT:C128806
Orphanet:181428
SCTID:238080004
UMLS:C0342883
MONDO:0015903
High level summary of knowledge for a disease, including descriptions and datasource references.