|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset.
|SAR1B||secretion associated, Ras related GTPase 1B||2.88009|