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| Term | spermatogenic failure 27 | ID (Ontology) | DOID:0111928 (Human Disease) |
| Definition | A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella, loss of the central pair of microtubules, loss of the inner dynein arms, and peripheral doublet disorganization of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in AK7 on chromosome 14q32.2. | ||
| Also Known As | "SPGF27" | ||
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autosomal genetic disease |__autosomal recessive disease__ male infertility | |__spermatogenic failure________| spermatogenic failure 27 |
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autosomal recessive disease spermatogenic failure |
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| MIM:617965 | |||