Search Ontology:
Human Disease

familial hypobetalipoproteinemia 2

Term ID
DOID:0111061
Synonyms
  • combined familial hypolipidemia
  • FHBL2
Definition
A hypobetalipoproteinemia that has_material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31. https://www.ncbi.nlm.nih.gov/pubmed/20942659
References
Ontology
Human Disease   ( DOID:0111061 )
Relationships
is a type of
disjoint_from
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.