Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6901
Gene Symbol: TAZ
TAZ
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2 		0.800 GermlineCausalMutation ORPHANET Mutations in the TAZ gene on chromosome Xq28, also known as G4.5, are responsible for the BTHS phenotype resulting in a loss-of-function in the protein product tafazzin. 23843353

2013
Entrez Id: 6901
Gene Symbol: TAZ
TAZ
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		0.300 GermlineCausalMutation ORPHANET The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. 9382096

1997
Entrez Id: 6901
Gene Symbol: TAZ
TAZ
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		0.300 GermlineCausalMutation ORPHANET X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. 7616547

1995