Disease: IMMUNODEFICIENCY 49 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310656
Disease: IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 49 		0.700 GeneticVariation disease UNIPROT BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells. 29985992 2018
CUI: C4310656
Disease: IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 49 		0.700 Biomarker disease GENOMICS_ENGLAND Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. 27959755 2016
CUI: C4310656
Disease: IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 49 		0.700 GeneticVariation disease UNIPROT Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. 27959755 2016
CUI: C4310656
Disease: IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 49 		0.700 CausalMutation disease CLINVAR
CUI: C4310656
Disease: IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 49 		0.700 Biomarker disease CTD_human