UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
F F F- F0 FA FB FC FD FE FF FG FH FI FJ FK FL FM FN FO FP FR FS FT FU FX FY
FA FAA FAB FAC FAD FAE FAI FAK FAL FAM FAN FAP FAR FAS FAT FAU FAV FAX

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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