Medical Definition of Familial chylomicronemia syndrome

1. An inherited disorder resulting in accumulation of chylomicrons as well as triacylglycerols. See: chylomicronemia. (05 Mar 2000)

Familial Chylomicronemia Syndrome Pictures

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Lexicographical Neighbors of Familial Chylomicronemia Syndrome

familial Mediterranean fever
familial adenomatous polyposis
familial aggregation
familial amyloid neuropathy
familial amyloidosis
familial aortic ectasia
familial aortic ectasia syndrome
familial bipolar mood disorder
familial breast cancer
familial cancer
familial chylomicronemia syndrome (current term)
familial combined hyperlipemia
familial combined hyperlipidaemia
familial dysbetalipoproteinaemia
familial emphysema
familial erythroblastic anaemia
familial fat-induced hyperlipaemia
familial glycinuria
familial goiter
familial high density lipoprotein deficiency
familial hyperbetalipoproteinaemia
familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia
familial hypercholesteraemic xanthomatosis
familial hypercholesterolaemia

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