ADA2, adenosine deaminase 2, 51816

N. diseases: 165; N. variants: 22
Disease: Sneddon Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 AlteredExpression disease BEFREE ADA2 activity in plasma and serum IgM concentrations was measured in adult patients within the SnS spectrum, healthy first-degree relatives and HC. 30645994 2018
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 GeneticVariation disease UNIPROT Mutant ADA2 in vasculopathies. 25075847 2014
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 GermlineCausalMutation disease ORPHANET Mutant ADA2 in vasculopathies. 25075847 2014
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 GermlineCausalMutation disease ORPHANET Sneddon's syndrome: a comprehensive review of the literature. 25551694 2014
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 Biomarker disease GENOMICS_ENGLAND Sneddon's syndrome. 3471198 1986
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 CausalMutation disease CLINVAR
CUI: C0282492
Disease: Sneddon Syndrome
Sneddon Syndrome 		0.710 Biomarker disease CTD_human