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inborn lipid/lipoprotein disorder
[genetically determined biochemical disorders in lipid/lipoprotein transport, apolipoprotein synthesis, HDL synthesis, enzyme deficiency or gene mutation that involves the lipid/lipoprotein metabolism pathway. ( CSP )]
UMLS (CSP) C0178714- Disease or Syndrome
Relation/PAR: Congenital Metabolic Disorder
Alteracoes do metabolismo lipidico
Alteracoes do metabolismo lipidico
Relation/CHD: inborn lipid storage disorder
RSH Syndrome
familial hypolipoproteinemia
familial hyperlipoproteinemia
RSH Syndrome
familial hypolipoproteinemia
familial hyperlipoproteinemia
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