OBO ID: DOID:0111062
Term Name: familial hypobetalipoproteinemia 1 Search Ontology:
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 familial hypobetalipoproteinemia 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
APOB Hypobetalipoproteinemia 615558
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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