Search Ontology:
Human Disease

chylomicron retention disease

Term ID
DOID:0060357
Synonyms
  • Anderson disease
  • CMRD
Definition
A lipid metabolism disorder characterized by malnutrition, failure to thrive, growth failure, vitamin E deficiency and the absence of chylomicrons and apolipoprotein B48 post-prandially. It has an autosomal recessive inheritance pattern and has_material_basis_in mutations in the SAR1B gene on chromosome 5q31.1. (5)
References
Ontology
Human Disease   ( DOID:0060357 )
Relationships
is a type of
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Genes Involved
Zebrafish Models