TRG, T cell receptor gamma locus, 6965

N. diseases: 54; N. variants: 0
Disease: Greig cephalopolysyndactyly syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265306
Disease: Greig cephalopolysyndactyly syndrome
Greig cephalopolysyndactyly syndrome 		0.010 GeneticVariation disease BEFREE Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes. 1981052 1990