1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070567 | spermatogenic failure 68 | A spermatogenic failure characterized by partial globozoospermia that has_material_basis_in homozygous mutation in the C2CD6 gene on chromosome 2q33.1. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |