Chylomicron retention disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Chylomicron retention disease (CRD) is a type of familial hypocholesterolemia characterized by malnutrition, failure to thrive, growth failure, vitamin E deficiency and hepatic, neurologic and ophthalmologic complications. (Orphanet Rare Disease Ontology, Orphanet_71)
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1 genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SAR1B secretion associated, Ras related GTPase 1B 2.88009