Spermatogenic Failure 36
Disease ID: disease_node_15172
Connections displayed (default: 10).
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| Dbxref | MIM:618420 |
|---|---|
| Subclassof | DOID_0050736, DOID_0111910 |
| Data Source | DOID |
| Synonyms | SPGF36 |
| Doid Label | spermatogenic failure 36 |
| Doid Description | A spermatogenic failure characterized by spermatozoa showing anomalies of the head, acrosome, and nucleus of the sperm resulting in reduced fertility that has_material_basis_in heterozygous mutation in the PPP2R3C gene on chromosome 14q13.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15172 |
| Doid Id | DOID_0111921 |
| Label | Spermatogenic Failure 36 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spermatogenic Failure(ID:disease_node_15133) (Disease)