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

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000021613 see paper; cardioprotective effect; lower fasting and postprandial serum triglycerides, higher levels HDL-cholesterol, lower levels LDL-cholesterol - - Familial, autosomal dominant - - - - - Johan den Dunnen 00025497
0000021614 see paper; associated with lower-TG (half) and higher HDL-C (>20%); reported as cardio-protective lipid profiles - - Familial, autosomal dominant - - - - - Johan den Dunnen 00025496
0000021615 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 - - Familial, autosomal dominant - - - - - Johan den Dunnen 00025498
0000021616 see paper; 0.3-0.4 reduced APOC3 plasma concentrations - - Familial, autosomal dominant - - - - - Johan den Dunnen 00025499
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