ADA, adenosine deaminase, 100

N. diseases: 379; N. variants: 61
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 		0.510 GeneticVariation disease BEFREE Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848 2011
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		0.510 GermlineCausalMutation disease ORPHANET
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		0.510 Biomarker disease GENOMICS_ENGLAND