| Disease ID | Source | Name | Description |
| 618643 | OMIM | Spermatogenic failure 39 (SPGF39) | An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic anomalies including short, absent, irregularly shaped and coiled flagella, and abnormalities of the head and midpiece. The disease is caused by variants affecting the gene represented in this entry. |