{"orpha":399775,"name":"Male infertility with spermatogenesis disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-399775/","orphanet_url":"https://www.orpha.net/en/disease/detail/399775","names":{"fr":{"name":"Infertilité masculine avec une anomalie de la spermatogenèse"},"de":{"name":"Männliche Infertilität mit Störung der Spermatogenese"},"es":{"name":"Infertilidad masculina con un trastorno de la espermatogénesis"},"it":{"name":"Sterilità maschile con difetto della spermatogenesi"},"nl":{"name":"Mannelijke onvruchtbaarheid met stoornis van spermatogenese"},"pt":{"name":"Infertilidade masculina com alteração de espermatogénese"},"pl":{"name":"Niepłodność męska z powodu zaburzeń spermatogenezy"},"cs":{"name":"Mužská neplodnost s poruchami spermatogeneze"},"uk":{"name":"Чоловіче безпліддя з порушенням сперматогенезу"},"zh":{"name":"男性不育伴生精障碍"},"tr":{"name":"Spermatogenez bozukluğu ile seyreden erkek infertilitesi"}},"xrefs":[{"source":"MONDO","code":"18391","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681167","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":399771,"name":"Male infertility due to sperm disorder","classifications":[156,201]}],"children":[{"orpha":1646,"name":"Chromosome Y microdeletion syndrome","type":"Malformation syndrome"},{"orpha":399786,"name":"Male infertility with spermatogenesis disorder due to single gene mutation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}