{"orpha":399882,"name":"Rare female infertility due to an implantation defect","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-399882/","orphanet_url":"https://www.orpha.net/en/disease/detail/399882","names":{"fr":{"name":"Infertilité féminine rare due à un défaut d'implantation"},"de":{"name":"Seltene weibliche Infertilität durch Implantationsdefekt"},"es":{"name":"Infertilidad femenina rara por un defecto en la implantación"},"it":{"name":"Sterilità femminile da difetto di impianto"},"nl":{"name":"Zeldzame vrouwelijke onvruchtbaarheid door implantatiedefect"},"pt":{"name":"Infertilidade feminina por defeito de implantação"},"pl":{"name":"Niepłodność żeńska z powodu nieprawidłowej implantacji"},"cs":{"name":"Ženská neplodnost způsobená poruchou implantace"},"uk":{"name":"Рідкісне жіноче безпліддя, зумовлене дефектом імплантації"},"zh":{"name":"植入缺陷所致罕见女性不育"},"tr":{"name":"İmplantasyon defektine bağlı nadir kadın infertilitesi"}},"xrefs":[{"source":"MONDO","code":"18403","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681135","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98049,"name":"Rare female infertility","classifications":[201]}],"children":[{"orpha":180142,"name":"Absence of uterine body","type":"Morphological anomaly"},{"orpha":1916,"name":"Diethylstilbestrol syndrome","type":"Malformation syndrome"},{"orpha":3109,"name":"Mayer-Rokitansky-Küster-Hauser syndrome","type":"Malformation syndrome"},{"orpha":180122,"name":"Septate uterus","type":"Clinical group"},{"orpha":180145,"name":"Uterine cervical aplasia and agenesis","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}