APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
Disease: Hypobetalipoproteinemia, Familial, 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1857970
Disease: Hypobetalipoproteinemia, Familial, 2
Hypobetalipoproteinemia, Familial, 2 		0.200 Biomarker disease MGD Regulation of the apolipoprotein B in heterozygous hypobetalipoproteinemic knock-out mice expressing truncated apoB, B81. Low production and enhanced clearance of apoB cause low levels of apoB. 10705993 1999
CUI: C1857970
Disease: Hypobetalipoproteinemia, Familial, 2
Hypobetalipoproteinemia, Familial, 2 		0.200 Biomarker disease MGD Two distinct apolipoprotein B alleles in mice generated by a single 'in-out' targeting. 8921909 1996