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| Term | spermatogenic failure 82 | ID (Ontology) | DOID:0070581 (Human Disease) |
| Definition | A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella that has_material_basis_in homozygous mutation in the AKAP3 gene on chromosome 12p13.32. | ||
| Also Known As | "SPGF82" | ||
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autosomal genetic disease |__autosomal recessive disease__ male infertility | |__spermatogenic failure________| spermatogenic failure 82 |
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| Is a |
autosomal recessive disease spermatogenic failure |
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| MIM:620353 | |||