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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 26-01-2009 |
Symbol | WATS | |||||
Location | 17q11.2 | |||||
Name | Watson syndrome | |||||
Other name(s) | cafe-au-lait spots with pulmonic stenosis | |||||
Corresponding gene | NF1 | |||||
Main clinical features |
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Genetic determination
Function/system disorder
| neurology |
| dermatology | Type
| disease
| |
Gene product |
Name | neurofibromin |
Remark(s) |