1 => The disorder is placed on the map based on its association with a gene, but the underlying defect is not known
2 => The disorder has been placed on the map by linkage; no mutation has been found
3 => The molecular basis for the disorder is known; a mutation has been found in the gene
4 => A contiguous gene deletion or duplication syndrome, multiple genes are deleted or duplicated causing the phenotype
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| EYA1 | 8q13.3 | 601653 | REc, Fd, Ch | Branchiootorenal syndrome 1, with or without cataracts, 113650 (3) | 113650 | 3 |
| EYA1 | 8q13.3 | 601653 | REc, Fd, Ch | Anterior segment anomalies with or without cataract, 602588 (3) | 602588 | 3 |
| EYA1 | 8q13.3 | 601653 | REc, Fd, Ch | Branchiootic syndrome 1, 602588 (3) | 602588 | 3 |
| EYA1 | 8q13.3 | 601653 | REc, Fd, Ch | ?Otofaciocervical syndrome, 166780 (3) | 166780 | 3 |