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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 24-03-2020 |
Symbol | LVNC |
Location | 18q12.1 |
Name | noncompaction of left ventricular myocardium, familial isolated |
Corresponding gene | DTNA |
Main clinical features | prominent left-ventricular trabeculae and deep intertrabecular recesses |
Genetic determination | autosomal dominant |
Related entries | DEL1P36 |
Function/system disorder | cardiovascular |
Type | disease |
Gene product |
Name | alpha-dystrobrevin |
Remark(s) | LVNC was reported in at least 12 cases of del1p36, suggesting that a gene in 1p36 might be responsible for LVNC |