Spermatogenic Failure 42
Disease ID: disease_node_15171
Connections displayed (default: 10).
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| Dbxref | MIM:618745 |
|---|---|
| Subclassof | DOID_0050737, DOID_0111910 |
| Data Source | DOID |
| Synonyms | SPGF42 |
| Doid Label | spermatogenic failure 42 |
| Doid Description | A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severly impaired sperm progressive motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the TTC29 gene on chromosome 4q31.22. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15171 |
| Doid Id | DOID_0111923 |
| Label | Spermatogenic Failure 42 |
- 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)