RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Congenital unilateral absence ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332909
Disease: Congenital unilateral absence
Congenital unilateral absence 		0.010 GeneticVariation disease BEFREE A GNDF mutation was identified in only one fetus with unilateral agenesis; this subject also had two RET mutations. 18252215 2008