Clinical genomic medicine

at the Centre for Rare Diseases at the MHH

The majority of rare diseases are caused by a genetic change in an inherited trait. However, it is not always possible to identify these causative gene variants in standard outpatient care as part of diagnostic genetic examinations. Thanks to the cooperation between the Institute of Human Genetics and the ZSE, the MHH is currently able to offer patients with rare diseases the additional option of detailed genetic testing: the"Model project for comprehensive diagnostics and therapy finding using genome sequencing in rare and oncological diseases".

Further information and details on registration can be found on the following page:
https://www.mhh.de/humangenetik/diagnostik-einsendungen/modellvorhaben-se