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GENATLAS PHENOTYPE |
last update : 13/07/2006 |
Symbol | INVM |
Location | Xq28 |
Name | noncompaction of the left ventricular myocardium, familial isolated |
Corresponding gene | TAZ |
Other symbol(s) | LVNC2, LVNCX |
Main clinical features | without features of Barth syndrome but allelic to it |
Genetic determination | sex linked |
Function/system disorder | cardiovascular |
Type | disease |
Gene product |
Name | tafazzin (TAZ) |