Xanthine dehydrogenase and aldehyde oxidase combined deficiency of; XDH and AOX dual deficiency; Type 2 Xanthinuria; Xanthine dehydrogenase and aldehyde oxidase combined deficiency of; XDH and AOX dual deficiency; Type 2 Xanthinuria; Type II XanthinuriaSee More
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
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Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
PubMed is a searchable database of medical literature and lists journal articles that discuss Xanthinuria type 2. Click on the link to view a sample search on this topic.