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
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CH CH1 CHA CHC CHD CHE CHG CHH CHI CHK CHL CHN CHO CHP CHR CHS CHU CHV CHY

cholesterol ester storage disease

[rare benign adult form of inherited lysosomal lipid storage disease that is due to deficiency of acid lipase; results in an accumulation of neutral lipids, particularly cholesterol esters, within cells (particularly leukocytes, fibroblasts, and liver cells); it is an allelic variant of Wolman disease. ( CSP )]
UMLS (CSP) C0008384
 
Disease or Syndrome
Relation/PAR: inborn lipid storage disorder
inborn lysosomal enzyme disorder


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