| Disease ID | Source | Name | Description |
| 616950 | OMIM | Spermatogenic failure, 15 (SPGF15) | An infertility disorder caused by spermatogenesis defects and characterized by non-obstructive azoospermia due to complete meiotic maturation arrest. SPGF15 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |
| 616947 | OMIM | Premature ovarian failure 12 (POF12) | An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol. The disease is caused by variants affecting the gene represented in this entry. |