Disease ID | Source | Name | Description |
618429 | OMIM | Spermatogenic failure 37 (SPGF37) | An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities, primarily consisting of short or absent flagella, and neck defects at the head-tail junction. The disease is caused by variants affecting the gene represented in this entry. |