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| Term | spermatogenic failure 44 | ID (Ontology) | DOID:0112109 (Human Disease) |
| Definition | A spermatogenic failure characterized by high prevalence of acephalic sperm and reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the CEP112 gene on chromosome 17q24.1. | ||
| Also Known As | "SPGF44" | ||
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autosomal genetic disease |__autosomal recessive disease__ male infertility | |__spermatogenic failure________| spermatogenic failure 44 |
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| Is a |
autosomal recessive disease spermatogenic failure |
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| MIM:619044 | |||