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| Term | spermatogenic failure 80 | ID (Ontology) | DOID:0070579 (Human Disease) |
| Definition | A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella, resulting in reduced or absent progressive sperm motility, that has_material_basis_in homozygous mutation in the DRC1 gene on chromosome 2p23.3. | ||
| Also Known As | "SPGF80" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ male infertility | |__spermatogenic failure________| spermatogenic failure 80 1 rec. |
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| Is a |
autosomal recessive disease spermatogenic failure |
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| MIM:620222 | |||