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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 23/06/2006 |
Symbol | DFNA39 |
Location | 4q22.1 |
HGNC id | 13833 |
Name | neurosensory deafness 39 |
Other name(s) |
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Corresponding gene | DSPP |
Main clinical features | with dentinogenesis imperfecta 1 |
Genetic determination | autosomal dominant |
Function/system disorder | ear |
Type | disease |
Remark(s) |