spermatogenic failure 8
Information
- Disease name
- spermatogenic failure 8
- Disease ID
- DOID:0070169
- Description
- "A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33." [url:https\://www.ncbi.nlm.nih.gov/pubmed/20887963]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0111910
- Cross Reference ID (Disease Ontology)
- MIM:613957
- Exact Synonym (Disease Ontology)
- SPGF8