familial cholesteryl ester deficiency

[disease characterized by abnormally low levels of plasma lecithin cholesterol acyl transferase; clinical manifestations include corneal opacity, anemia, and proteinuria. ( CSP )]

UMLS (CSP) C0023195

Disease or Syndrome

Relation/PAR: hypolipoproteinemia
enzyme deficiency
familial hypolipoproteinemia

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