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Arthrogryposis multiplex congenita, distal type 2
Other Names for this Disease
- Congenital contractures with major involvement of the hands and feet
- Distal arthrogryposis, type 2
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In Depth Information
- The Online Mendelian Inheritance in Man (OMIM) is an 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.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Arthrogryposis multiplex congenita, distal type 2. Click on the link to view a sample search on this topic.