Disease: IMMUNODEFICIENCY 22 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4014233
Disease: IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 22 		0.700 GeneticVariation disease UNIPROT Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency. 22985903 2012
CUI: C4014233
Disease: IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 22 		0.700 Biomarker disease GENOMICS_ENGLAND Defect of lck in a patient with common variable immunodeficiency. 11351273 2001
CUI: C4014233
Disease: IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 22 		0.700 GermlineCausalMutation disease ORPHANET
CUI: C4014233
Disease: IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 22 		0.700 Biomarker disease CTD_human
CUI: C4014233
Disease: IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 22 		0.700 CausalMutation disease CLINVAR