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cholesterol-ester transfer protein deficiency | RareConnect | RareConnect.io

/familial hyperlipidemia

/hyperalphalipoproteinemia

/cholesterol-ester transfer protein deficiency

cholesterol-ester transfer protein deficiency

Rare Disease

MONDO:0007744

Also Known As

hyperalphalipoproteinemiaCEPT deficiencyfamilial hyperalphalipoproteinemiahigh density lipoprotein cholesterol level QTL 10hyperalphalipoproteinemia 1hyperalphalipoproteinemia type 1CETP deficiencyHALP1Hdlcq10cholesterol ester transfer Protein deficiencyhigh density lipoprotein cholesterol level quantitative trait locus 10

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:143470 ↗

Orphanet

Orphanet:79506 ↗

GARD

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