Links to patient organization

Patient organizations dedicated to homocystinurias

Many other national patient associations offer support to patients with homocystinurias, methylation and remethylation disorders, and to their families. National contact points may be found on the website of umbrella organizations:

 

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.
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E-HOD has been funded by the European Commission through its Public Health and Consumer Protection Directorate (DG SANCO), PHEA programme (more information).
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