Disease #03520 (apolipoprotein C-III deficiency (hyperalphalipoproteinemia, type 2 (HALP-2)), OMIM:614028)

Official abbreviation -
Name apolipoprotein C-III deficiency (hyperalphalipoproteinemia, type 2 (HALP-2))
OMIM ID 614028
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene APOC3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2016-07-05 08:24:40 +02:00 (CEST)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00025496 - PubMed: Crawford 2014 samples from NHANES study - - United States - - - - - apolipoprotein C-III deficiency (hyperalphalipoproteinemia, type 2 (HALP-2)) see paper; associated with lower-TG (half) and higher HDL-C (>20%); reported as cardio-protective lipid profiles APOC3 APOC3 1 31 Johan den Dunnen
00025497 - PubMed: Pollin 2008 - - - United States Amish (Lancaster) - - - - apolipoprotein C-III deficiency (hyperalphalipoproteinemia, type 2 (HALP-2)) see paper; cardioprotective effect; lower fasting and postprandial serum triglycerides, higher levels HDL-cholesterol, lower levels LDL-cholesterol APOC3 APOC3 1 59 Johan den Dunnen
00025498 - PubMed: Maeda 1987 2-generation family, 3 affecteds - no Japan - - - - - apolipoprotein C-III deficiency (hyperalphalipoproteinemia, type 2 (HALP-2)) see paper; raised apolipoprotein C-III-O levels; normal triacylglycerols/cholesterol concentrations of VLDL, low density lipoprotein (LDL), HDL fractions, serum apolipoprotein C-III levels APOC3 APOC3 1 3 Johan den Dunnen
00025499 - PubMed: von Eckardstein 1991 2-generation family, mother and daugther F no Germany - - - - - apolipoprotein C-III deficiency (hyperalphalipoproteinemia, type 2 (HALP-2)) see paper; 0.3-0.4 reduced APOC3 plasma concentrations APOC3 APOC3 1 2 Johan den Dunnen
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