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X-linked spermatogenic failure 2
Summary
- Synonym
-
- SPGFX2
- Definition
- A spermatogenic failure that is characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has_material_basis_in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13.
- Super Class
- X-linked recessive disease spermatogenic failure
External Links
- Disease Ontology
- DOID:0070185
- Mondo Disease Ontology
- OMIM
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0008669 | Abnormal spermatogenesis |
| HP:0000118 | Phenotypic abnormality |
| HP:0011961 | Non-obstructive azoospermia |
| HP:0000027 | Azoospermia |
| HP:0008734 | Decreased testicular size |
| HP:0011962 | Obstructive azoospermia |
| HP:0000837 | Increased circulating gonadotropin level |
