E-HOD Consortium cannot provide clinical advice for patients, if you are a patient or a family member, please, seek a help from your health care provider. If you are searching for a patient support group, you can find more details here.

Please, select the appropriate topic and your request will be directed to relevant persons within the E-HOD consortium.

This is E-HOD

European network and registry for homocystinurias and methylation defects. Its aim is to improve the health of children, adolescents and adults affected with these rare disorders.
E-HOD has been funded by the European Commission through its Public Health and Consumer Protection Directorate (DG SANCO), PHEA programme (more information).