Search Ontology:
Human Disease

familial hypobetalipoproteinemia 1

Term ID
DOID:0111062
Synonyms
  • FHBL1
Definition
A hypobetalipoproteinemia that has_material_basis_in mutation in the APOB gene on chromosome 2p24. https://www.ncbi.nlm.nih.gov/pubmed/3399894
References
Ontology
Human Disease   ( DOID:0111062 )
Relationships
is a type of
inverse disjoint_from
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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