has material basis in germline mutation in CETP familial hyperlipidemia cholesterol-ester transfer protein deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/hyperalphalipoproteinemia_1 hyperalphalipoproteinemia SCTID:15771000119109 DOID:0111369 OMIM:143470 CEPT deficiency familial hyperalphalipoproteinemia MONDO:0007744 UMLS:C3875011 hyperalphalipoproteinemia 1 hyperalphalipoproteinemia type 1 high density lipoprotein cholesterol level QTL 10 GARD:0016724 MEDGEN:840020 Orphanet:79506 HALP1 hyperalphalipoproteinemia