{"orpha":399771,"name":"Male infertility due to sperm 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-399771/","orphanet_url":"https://www.orpha.net/en/disease/detail/399771","names":{"fr":{"name":"Infertilité masculine due à une anomalie du sperme"},"de":{"name":"Männliche Infertilität, Spermien-abhängige"},"es":{"name":"Infertilidad masculina por un trastorno del esperma"},"it":{"name":"Sterilità maschile da anomalie spermatiche"},"nl":{"name":"Mannelijke onvruchtbaarheid door spermastoornis"},"pt":{"name":"Infertilidade masculina por alteração do esperma"},"pl":{"name":"Niepłodność męska z powodu zaburzeń nasienia"},"cs":{"name":"Mužská neplodnost způsobená abnormalitami spermatu"},"uk":{"name":"Чоловіче безпліддя, зумовлене порушенням спермограми"},"zh":{"name":"精子异常所致男性不育"},"tr":{"name":"Sperm bozukluğuna bağlı erkek infertilitesi"}},"xrefs":[{"source":"MONDO","code":"18390","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681162","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":399764,"name":"Male infertility due to gonadal dysgenesis or sperm disorder","classifications":[156,201]}],"children":[{"orpha":399813,"name":"Male infertility due to sperm motility disorder","type":"Category"},{"orpha":399775,"name":"Male infertility with spermatogenesis disorder","type":"Category"},{"orpha":33364,"name":"Trichothiodystrophy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}