Spermatogenic Failure 48
Disease ID: disease_node_15161
Connections displayed (default: 10).
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| Dbxref | MIM:619108 |
|---|---|
| Subclassof | DOID_0050737, DOID_0111910 |
| Data Source | DOID |
| Synonyms | SPGF48 |
| Doid Label | spermatogenic failure 48 |
| Doid Description | A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15161 |
| Doid Id | DOID_0112176 |
| Label | Spermatogenic Failure 48 |
- 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)