The GenCC develops consistent terminology for describing gene-disease validity. As part of the GenCC we are aligning our existing terms to the new terminology.
We are planning to move to the new terminology this autumn. Please find out more about the planned update here.
For example: CRYBA1, ZEB2, TBX1, CHANARIN-DORFMAN SYNDROME or Severe Neurodevelopmental Syndrome
|Gene symbol||Genotype||Mutation consequence||Disease||Panels||Go to page|
|ARHGEF9||x-linked dominant||loss of function||ARHGEF9-related developmental disorder (X-linked dominant)||DD|