| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/204690 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the amelogenesis imperfecta, type ig (enamel-renal syndrome) phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FAM20A | family with sequence similarity 20, member A |
