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| Term | spermatogenic failure 6 | ID (Ontology) | DOID:0070167 (Human Disease) |
| Definition | A male infertility characterized by autosomal recessive inheritance of globozoospermia that has_material_basis_in mutation in the SPATA16 gene on chromosome 3q26. | ||
| Also Known As | "SPGF6" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal recessive disease______________ spermatogenic failure | |__male infertility due to globozoospermia__| spermatogenic failure 6 |
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| Is a |
autosomal recessive disease male infertility due to globozoospermia |
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External Crossreferences & Linkouts
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MESH:D000072660 MIM:102530 NCI:C158500 |
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