{"orpha":399813,"name":"Male infertility due to sperm motility disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Male infertility due to asthenozoospermia"],"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-399813/","orphanet_url":"https://www.orpha.net/en/disease/detail/399813","names":{"fr":{"name":"Infertilité masculine due à un défaut de motilité"},"de":{"name":"Männliche Infertilität durch Störung der Spermienmotilität","synonyms":["Männliche Infertilität durch Asthenozoospermie"]},"es":{"name":"Infertilidad masculina por un trastorno de motilidad del esperma","synonyms":["Infertilidad masculina por astenozoospermia"]},"it":{"name":"Sterilità maschile da difetto della motilità spermatica","synonyms":["Sterilità maschile da astenozoospermia"]},"nl":{"name":"Mannelijke onvruchtbaarheid door stoornis van spermamotiliteit","synonyms":["Mannelijke onvruchtbaarheid door asthenozoöspermie"]},"pt":{"name":"Infertilidade masculina por alteração da motilidade espermática"},"pl":{"name":"Niepłodność męska z powodu zaburzeń ruchliwości plemników","synonyms":["Niepłodność męska z powodu astenozoospermii"]},"cs":{"name":"Mužská neplodnost způsobená nedostatečnou pohyblivostí spermií","synonyms":["Mužská neplodnost způsobená astenozoospermií"]},"uk":{"name":"Чоловіче безпліддя, зумовлене порушенням рухливості сперматозоїдів","synonyms":["Чоловіче безпліддя через астенозооспермію"]},"zh":{"name":"精子运动障碍导致的男性不育","synonyms":["弱精子症所致男性不育"]},"tr":{"name":"Sperm motilite bozukluğuna bağlı erkek infertilitesi","synonyms":["Astenozoospermiye bağlı erkek infertilitesi"]}},"xrefs":[{"source":"MONDO","code":"18395","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680032","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":94064,"name":"Deafness-infertility syndrome","type":"Malformation syndrome"},{"orpha":276234,"name":"Non-syndromic male infertility due to sperm motility disorder","type":"Disease"},{"orpha":244,"name":"Primary ciliary dyskinesia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}