Version: 8.0.0
Date: Tue Jan 28 2025
familial hypobetalipoproteinemia 2
DOID:0111061
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

familial hypobetalipoproteinemia 2

Definition
A hypobetalipoproteinemia that has_material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31.
Synonyms
  • combined familial hypolipidemia
  • FHBL2
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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