(Q27677584)
English
achromatopsia 3
An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.
- ACHM1
- ACHM3
- Pingelapese blindness
- RMCH1
- rod monochromacy 1
- rod monochromatism 1
- Rod Monochromacy 1, Formerly
- Achm1, Formerly
- Total Colorblindness With Myopia
- Achromatopsia With Myopia
- ACHROMATOPSIA 3
- Achromatopsia type 3
- Rod Monochromatism 1, Formerly
- ACHROMATOPSIA 3; ACHM3
Statements
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Identifiers
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