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Echinobase
Summary Literature (0)
DOID:0111061 - familial hypobetalipoproteinemia 2

Disease Ontology Definition:A hypobetalipoproteinemia that has material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31.

Synonyms: FHBL2, combined familial hypolipidemia,

Echinobase Genes :


OMIM:
MIM:605019 - hypobetalipoproteinemia, familial, 2; fhbl2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypobetalipoproteinemia (is_a)