| Disease ID | Source | Name | Description |
| 618091 | OMIM | Spermatogenic failure 29 (SPGF29) | An autosomal recessive infertility disorder caused by spermatogenesis defects that result in non-obstructive azoospermia or oligozoospermia. When produced, spermatozoa are immotile and have abnormal morphology, primarily defects of the acrosome and head-neck junction. The disease is caused by variants affecting the gene represented in this entry. |