| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/202110 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CYP17A1 | cytochrome P450, family 17, subfamily A, polypeptide 1 |
