List of diseases covered by
Frazer Syndrome NGS panel
| Gene | Condition |
| EYA1 | Otofaciocervical syndrome; Anterior segment anomalies with or without cataract; ranchiootic syndrome 1; Branchiootorenal syndrome 1, with or without cataracts |
| FREM1 | Bifid nose with or without anorectal and renal anomalies; Manitoba oculotrichoanal syndrome; Trigonocephaly 2 |
| FREM2 | Cryptophthalmos, unilateral or bilateral, isolated; Fraser syndrome 2 |
| FRAS1 | Fraser syndrome 1 |
| GRIP1 | Fraser syndrome 3 |
| SIX1 | Branchiootic syndrome 3; Deafness, autosomal dominant 23 |
| SIX5 | Branchiootorenal syndrome 2 |