Hiperlipidemia: Perbedaan antara revisi

! Perkiraan prevalensi

|-

| {{OMIM|238600||none}}

| Buerger-Gruetz syndrome or familial hyperchylomicronemia

| rowspan="3" | One in 1,000,000<ref>{{cite web | title = Hyperlipoproteinemia, Type I | date = 6 March 2007 | url = http://www.cags.org.ae/FMPro?-DB=ctga.fp5&-Format=ctga%2Fctga_detail.html&-RecID=34563&-Find | archive-url = https://web.archive.org/web/20120327213629/http://www.cags.org.ae/FMPro?-DB=ctga.fp5&-Format=ctga%2Fctga_detail.html&-RecID=34563&-Find | archive-date=27 March 2012 | work = Centre for Arab Genomic Studies | quote = About 1:1,000,000 people are affected with Hyperlipoproteinemia type I worldwide with a higher prevalence in some regions of Canada. }}</ref>

|-

| {{OMIM|207750||none}}

| Familial apoprotein CII deficiency

| Altered [[apolipoprotein C2|ApoC2]]

|-

| {{OMIM|118830||none}}

|

| [[Lipoprotein lipase|LPL]] inhibitor in blood

|-

! a

| {{OMIM|143890||none}}

| One in 100

|-

| {{OMIM|107741||none}}

| [[Familial dysbetalipoproteinemia]]

| One in 10,000<ref name="fung2011">{{cite journal | vauthors = Fung M, Hill J, Cook D, Frohlich J | title = Case series of type III hyperlipoproteinemia in children | journal = BMJ Case Reports | volume = 2011 | pages = bcr0220113895 | date = June 2011 | pmid = 22691586 | pmc = 3116222 | doi = 10.1136/bcr.02.2011.3895 }}</ref>

|-

| {{OMIM|144600||none}}

| [[Familial hypertriglyceridemia]]

| One in 100

|-

| {{OMIM|144650||none}}

|