UNC13D, unc-13 homolog D, 201294

N. diseases: 48; N. variants: 26
Disease: Immune System Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.010 GeneticVariation group BEFREE Mutations in UNC13D cause the severe immune disorder familial haemophagocytic lymphohistiocytosis type 3 (FHL3). 21182842 2011