WormBase Tree Display for DO_term: DOID:0110007
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| DOID:0110007 | Name | achromatopsia 2 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11. | ||||
| Synonym | Exact | ACHM2 | |||
| RMCH2 | |||||
| rod monochromacy 2 | |||||
| rod monochromatism 2 | |||||
| Parent | Is_a | DOID:13911 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 216900 | |
| Attribute_of | Gene_by_orthology | WBGene00000487 | |||
| WBGene00006526 | |||||
| WBGene00022295 |
