Print friendly version
3 methylglutaconic aciduria type I
Other Names for this Disease
- 3 alpha methylglutaconic aciduria type I
- 3 methylglutaconyl CoA hydratase deficiency
- 3MG CoA hydratase deficiency
- MGA type I
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
Overview
These Web pages are updated as the Genetic and Rare Diseases Information Center
receives questions and as new information becomes available. If you don’t see
many information resources on this page, it may be because the Information Center
hasn’t yet received a question about this condition.
Your Questions Answered
by the Genetic and Rare Diseases Information CenterPlease contact us with your questions about 3 methylglutaconic aciduria type I. We will answer your question and update these pages with new resources and information.
On this page
General Information
- Genetics Home Reference (GHR) contains information on 3 methylglutaconic aciduria type I. Click on the link to go to GHR and review the information.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. Click on the link to read information on this topic.
- The The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss 3 methylglutaconic aciduria type I. Click on the link to go to OMIM and review these resources.