SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Cholesterin & Co e.V. - Patientenorganisation für Patienten mit Familiärer Hypercholesterinämie oder anderen schweren genetischen Fettstoffwechselstörungen Assigned diseases:

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In the following you will find the diseases that this support group organisation focuses on:
Abetalipoproteinemia Apolipoprotein A-I deficiency Cerebrotendinous xanthomatosis Cholesterol-ester transfer protein deficiency Cholesteryl ester storage disease Chylomicron retention disease Combined hyperlipidemia Dysbetalipoproteinemia Familial LCAT deficiency Familial apolipoprotein C-II deficiency Familial lipoprotein lipase deficiency Fish-eye disease Homozygous familial hypercholesterolemia Hyperalphalipoproteinemia Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency Hyperlipidemia due to hepatic triacylglycerol lipase deficiency Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 5 Hypoalphalipoproteinemia Hypobetalipoproteinemia LCAT deficiency Lipoprotein glomerulopathy Lysosomal acid lipase deficiency Rare dyslipidemia Rare hyperlipidemia Rare hypolipidemia Rare major hypertriglyceridemia Rare syndromic dyslipidemia Sitosterolemia Tangier disease Wolman disease