| Metadata | |
|---|---|
| ID | DOID:0070178 |
| Name | spermatogenic failure 10 |
| Definition | A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/22275165 |
| Xrefs | |
| Synonyms |
Spermatogenic failure with defective sperm annulus [EXACT] SPGF10 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |