HMOX1, heme oxygenase 1, 3162

N. diseases: 666; 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 Biomarker disease BEFREE We report another case of human HO-1 deficiency in a young girl with congenital asplenia, who presented with severe hemolysis, inflammation, nephritis, which was refractory to therapy with corticosteroids, cyclophosphamide, and rituximab. 21088618 2011