has material basis in germline mutation in SAR1B intestinal disorder chylomicron retention disease https://rarediseases.info.nih.gov/diseases/9683/chylomicron-retention-disease https://www.malacards.org/card/chylomicron_retention_disease hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells chylomicron retention disease CRD OMIM:246700 MESH:C535460 MONDO:0009528 CMRD Orphanet:71 Anderson disease MEDGEN:208651 GARD:0009683 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. UMLS:C0795956 icd11.foundation:1447416932 SCTID:702364003 DOID:0060357 obsolete intestinal disease due to fat malabsorption hypobetalipoproteinemia