Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7299
Gene Symbol: TYR
TYR
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I 		0.010 GeneticVariation BEFREE Tyrosinemia type I (TYRSN1, TYR I) is caused by fumarylacetoacetate hydrolase (FAH) deficiency and affects approximately one in 100,000 individuals worldwide. 27397503

2016