| Term Name: | achromatopsia 3 |
|---|---|
| Synonyms: | ACHM1, ACHM3, Pingelapese blindness, RMCH1, rod monochromacy 1, rod monochromatism 1 |
| Definition: | An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2. |
| Ontology: | Human Disease [DOID:0110008] ( DOID:0110008 ) |