HP, haptoglobin, 3240

N. diseases: 464; N. variants: 9
Disease: Congenital absence of spleen ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		0.010 GeneticVariation disease BEFREE Significant associations of specific Hp genotypes with comorbidities were also found, while results suggested that MPO AA homozygosis could increase effects of asplenia. 24567965 2014