Disease | dilated cardiomyopathy |
Phenotype | C0574083|barth syndrome |
Sentences | 2 |
PubMedID- 23031367 | Intrafamilial variability for novel taz gene mutation: barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle. |
PubMedID- 24116962 | The first disorder linked to abnormal mitochondrial lipid metabolism was barth syndrome of dilated cardiomyopathy associated with cyclical neutropenia, growth retardation and 3-methylglutaconic aciduria (clarke et al., 2013). |
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