CCR7, C-C motif chemokine receptor 7, 1236

N. diseases: 320; N. variants: 3
Disease: Radioulnar Synostosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		0.010 GeneticVariation disease BEFREE Radioulnar synostosis and B-cell deficiency were observed only in patients with mutations affecting a short region in the C-terminal zinc finger domain of EVI1. 29540340 2018