RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Congenital condition ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3649644
Disease: Congenital condition
Congenital condition 		0.010 GeneticVariation disease BEFREE Establishment of an induced pluripotent stem cell model of Hirschsrpung disease, a congenital condition of the enteric nervous system, from a patient carrying a novel RET mutation. 29965875 2018