Disease: Omenn Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		0.300 Biomarker disease GENOMICS_ENGLAND CD45-deficient severe combined immunodeficiency caused by uniparental disomy. 22689986 2012