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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 11-01-2017 |
Symbol | MROS2 |
Location | 19p13.11 |
Name | Melkersson-Rosenthal syndrome 2 |
Corresponding gene | SLC27A1 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | connective tissue |
dermatology | |
Type | disease |
Remark(s) |