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Disease Ontology Browser
familial hypobetalipoproteinemia 2 (DOID:0111061)
Alliance: disease page
Synonyms: combined familial hypolipidemia; FHBL2
Alt IDs: OMIM:605019
Definition: A hypobetalipoproteinemia that has_material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory