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DOID:0111062 - familial hypobetalipoproteinemia 1
Disease Ontology Definition:A hypobetalipoproteinemia that has_material_basis_in mutation in the APOB gene on chromosome 2p24.
Synonyms: FHBL1,
Xenbase Genes : apob
MONDO:0014252 - familial hypobetalipoproteinemia 1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypobetalipoproteinemia (is_a)