Other Names for this Disease
- Pingelapese blindness
- Achromatopsia with myopia
- Total colorblindness with myopia
- ACHM1 (formerly)
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.
- Genetics Home Reference (GHR) contains information on Achromatopsia 3. This website is maintained by the National Library of Medicine.
- 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.