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| Term | spermatogenic failure 61 | ID (Ontology) | DOID:0112350 (Human Disease) | |||||||||
| Definition | A spermatogenic failure that is characterized by male infertility due to nonobstructive azoospermia with complete meiotic arrest at the primary spermatocyte stage that has_material_basis_in homozygous or compound heterozygous mutation in the STAG3 gene on chromosome 7q22.1. | |||||||||||
| Also Known As | "SPGF61" | |||||||||||
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autosomal genetic disease |__autosomal recessive disease__ male infertility | |__spermatogenic failure________| spermatogenic failure 61 2 rec. |
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autosomal recessive disease spermatogenic failure |
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| MIM:619672 | |||