| Disease ID | Source | Name | Description |
| 618115 | OMIM | Spermatogenic failure 32 (SPGF32) | An autosomal dominant infertility disorder caused by spermatogenesis defects that result in non-obstructive azoospermia. The disease is caused by variants affecting the gene represented in this entry. |
| 617690 | OMIM | Ovarian dysgenesis 5 (ODG5) | A disorder characterized by lack of spontaneous pubertal development, primary amenorrhea, uterine hypoplasia, and hypergonadotropic hypogonadism as a result of streak gonads. ODG5 is an autosomal recessive condition. The disease is caused by variants affecting the gene represented in this entry. |