OBO ID: DOID:0070168 |
Term Name: | spermatogenic failure 3 | Search Ontology: | |
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Synonyms: |
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Definition: | A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/23582645 | ||
References: | |||
Ontology: | Human Disease ( DOID:0070168 ) |
OTHER spermatogenic failure 3 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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SLC26A8 | Spermatogenic failure 3 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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