1 => Disorder placed on map based on association with a gene; defect unknown
2 => Disorder placed by linkage; no mutation found
3 => Molecular basis known; mutation found in gene
4 => Contiguous gene deletion/duplication syndrome
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| EYA4 | 6q23.2 | 603550 | R, Fd, A | Deafness, autosomal dominant 10, 601316 (3) | 601316 | 3 |
| EYA4 | 6q23.2 | 603550 | R, Fd, A | ?Cardiomyopathy, dilated, 1J, 605362 (3) | 605362 | 3 |