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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Corneal endothelial dystrophy type 2


Other Names for this Disease

  • CHED2
  • Congenital hereditary endothelial dystrophy of the cornea
  • Corneal dystrophy, congenital hereditary endothelial
  • Maumenee corneal dystrophy
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 Center

1 question(s) from the public on Corneal endothelial dystrophy type 2 have been answered. See questions and answers. You can also submit a new question.
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In Depth Information

  • 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 Corneal endothelial dystrophy type 2. Click on the link to view a sample search on this topic.
Other Names for this Disease
  • CHED2
  • Congenital hereditary endothelial dystrophy of the cornea
  • Corneal dystrophy, congenital hereditary endothelial
  • Maumenee corneal dystrophy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.