Spermatogenic Failure 17
Disease ID: disease_node_15230
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| Dbxref | MIM:617214 |
|---|---|
| Subclassof | DOID_0050737, DOID_0111910 |
| Data Source | DOID |
| Synonyms | Male infertility due to oocyte activation failure, SPGF17 |
| Doid Label | spermatogenic failure 17 |
| Doid Description | A spermatogenic failure that is characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15230 |
| Doid Id | DOID_0070174 |
| Label | Spermatogenic Failure 17 |
- Outgoing r'ship
SUBCLASS_OFto/from Spermatogenic Failure(ID:disease_node_15133) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)