Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 09-10-2017 |
Symbol | MRX89 |
Location | Xp11.3 |
Name | mental retardation, 89 |
Corresponding gene | ZNF41 |
Main clinical features | nonsyndromic X-linked mental retardation, with language retardation, avoided social contact |
Genetic determination | sex linked |
Function/system disorder | mental retardation |
Type | disease |
Remark(s) |