HP, haptoglobin, 3240

N. diseases: 464; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 GeneticVariation disease BEFREE <b>Conclusions:</b> These results suggest that subjects with type 2 diabetes carrying the Hp 1-1 genotype may have higher susceptibility to depression in the context of white matter damage and frontal lobe atrophy. 30809196 2019
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 Biomarker disease BEFREE It seems advisable to assess the intestinal permeability using as a marker, for example, zonulin and specific IgG concentrations against selected nutritional components in patients with depression. 25268936 2017
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 Biomarker disease PSYGENET The patients with major depression exhibited significantly higher haptoglobin plasma levels than the healthy comparison subjects and the patients with minor depression. 8267107 1994
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 AlteredExpression disease BEFREE The patients with major depression exhibited significantly higher haptoglobin plasma levels than the healthy comparison subjects and the patients with minor depression. 8267107 1994
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 Biomarker disease PSYGENET Serum prealbumin and retinol-binding protein in the prealbumin-related senile and familial forms of systemic amyloidosis. 4038761 1985
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 Biomarker disease PSYGENET Haptoglobin types and unipolar depression. 6745954 1984
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 Biomarker disease BEFREE The results show virtually no evidence of linkage between depression spectrum disease and C3, but suggestive evidence (lod score = 1.03) of linkage between depression spectrum disease and alpha-haptoglobin (both these linkages were previously suggested by significant results in sib-pair analyses). 431798 1979
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 GeneticVariation disease BEFREE Preliminary data suggest the possibility of linkage between the alpha-haptoglobin locus and third component of complement locus and depression spectrum disease, a depression which is familially defined by the presence of alcoholism in the first-degree family member. 401356 1979
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.360 Biomarker disease BEFREE Preliminary data indicate that depression spectrum disease may be linked to such genetic markers as C3 or alpha-haptoglobin. 760696 1979