Spermatogenic Failure 11
Disease ID: disease_node_15223
Connections displayed (default: 10).
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| Dbxref | MIM:615081 |
|---|---|
| Subclassof | DOID_0050736, DOID_0111910 |
| Data Source | DOID |
| Synonyms | SPGF11 |
| Doid Label | spermatogenic failure 11 |
| Doid Description | A spermatogenic failure that is characterized by autosomal domit inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15223 |
| Doid Id | DOID_0070180 |
| Label | Spermatogenic Failure 11 |
- 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)