Spermatogenic Failure 39
Disease ID: disease_node_15169
Connections displayed (default: 10).
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| Dbxref | MIM:618643 |
|---|---|
| Subclassof | DOID_0050737, DOID_0111910 |
| Data Source | DOID |
| Synonyms | SPGF39 |
| Doid Label | spermatogenic failure 39 |
| Doid Description | A spermatogenic failure characterized by multiple morphologic anomalies of the sperm flagellum, lack of the outer dynein arms in the flagella, and asthenozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH17 gene on chromosome 17q25.3. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15169 |
| Doid Id | DOID_0111926 |
| Label | Spermatogenic Failure 39 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spermatogenic Failure(ID:disease_node_15133) (Disease)