achromatopsia 2 (Q27677583)
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An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
- ACHM2
- RMCH2
- rod monochromacy 2
- rod monochromatism 2
- achromatopsia type 2
- ACHROMATOPSIA 2
- Colorblindness, Total
- ACHROMATOPSIA 2; ACHM2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | achromatopsia 2 |
An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11. |
|
Statements
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Identifiers
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