HP, haptoglobin, 3240

N. diseases: 228; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.320 GeneticVariation group BEFREE The Hpt 2-2 phenotype is associated with increased prevalence of various systemic diseases, including autoimmune disorders. 20943062 2010
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.320 AlteredExpression group BEFREE Zonulin upregulation seems to precede the onset of the disease, providing a possible link between increased intestinal permeability, environmental exposure to non-self antigens, and the development of autoimmunity in genetically susceptible individuals. 16644703 2006
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.320 Biomarker group CTD_human Iron and infection: effects of host iron status and the iron-regulatory genes haptoglobin and NRAMP1 (SLC11A1) on host-pathogen interactions in tuberculosis and HIV. 16597321 2006