| Disease ID | Source | Name | Description |
| 618745 | OMIM | Spermatogenic failure 42 (SPGF42) | An autosomal recessive infertility disorder characterized by almost immotile spermatozoa due to multiple morphologic abnormalities of the flagella, including short, absent, coiled, and bent flagella. Some spermatozoa also show abnormalities of the head, acrosome, midpiece, or endpiece. The disease is caused by variants affecting the gene represented in this entry. |