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| Term | spermatogenic failure 5 | ID (Ontology) | DOID:0070183 (Human Disease) |
| Definition | A spermatogenic failure that is characterized by autosomal recessive inheritance of large-headed, multiflagellar, polyploid spermatozoa that has_material_basis_in mutation in the AURKC gene on chromosome 19q13. | ||
| Also Known As | "Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid" ; "infertility associated with multitailed spermatozoa and excessive DNA" ; "macrocephalic sperm head syndrome" (for all, see Synonyms field below) | ||
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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 5 2 rec. |
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| Is a |
autosomal recessive disease spermatogenic failure |
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External Crossreferences & Linkouts
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GARD:12385 MESH:C562903 MIM:243060 ORDO:137893 SNOMEDCT_US_2021_09_01:236806004 |
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