TTC7A, tetratricopeptide repeat domain 7A, 57217

N. diseases: 59; N. variants: 26
Disease: Hypergammaglobulinemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia 		0.010 GeneticVariation disease BEFREE Our findings should alert the physicians to consider screening of <i>TTC7A</i> mutations in patients with lymphoproliferative syndrome and hypergammaglobulinemia and/or chronic intestinal pseudo-obstruction. 31787977 2019