{"orpha":73217,"name":"Müllerian aplasia","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Aplasia of the Müllerian ducts","Müllerian duct failure"],"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-73217/","orphanet_url":"https://www.orpha.net/en/disease/detail/73217","names":{"fr":{"name":"Aplasie müllérienne","synonyms":["Aplasie des canaux de Müller"]},"de":{"name":"Müller-Gang-Aplasie"},"es":{"name":"Aplasia mulleriana","synonyms":["Ausencia de conducto mulleriano"]},"it":{"name":"Aplasia mülleriana","synonyms":["Insufficienza dei dotti mülleriani"]},"nl":{"name":"Mülleriaanse aplasie","synonyms":["Aplasie van gang van Müller"]},"pt":{"name":"Aplasia dos canais mullerianos","synonyms":["Insuficiência dos canais mullerianos"]},"pl":{"name":"Aplazja Mullera","synonyms":["Zaburzenie przewodów Mullera"]},"cs":{"name":"Mülleriánská aplázie","synonyms":["Selhání Müllerova vývodu","Aplázie Müllerových vývodů"]},"uk":{"name":"Мюллерова аплазія","synonyms":["Аплазія мюллерових проток","Порушення Мюллерової протоки"]},"zh":{"name":"苗勒管发育不全","synonyms":["米勒管发育不全"]},"tr":{"name":"Müllerian aplazisi","synonyms":["Müllerian kanal yetmezliği","Müllerian kanalların aplazisi"]}},"xrefs":[{"source":"MONDO","code":"0019128","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19128","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C537371","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0431637","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"7100","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":156622,"name":"Genetic urogenital tract malformation","classifications":[156]},{"orpha":180065,"name":"Non-syndromic uterovaginal malformation","classifications":[147,185,205,233]},{"orpha":183731,"name":"Rare genetic gynecological and obstetrical diseases","classifications":[156]}],"children":[{"orpha":180068,"name":"Partial bilateral aplasia of the Müllerian ducts","type":"Clinical group"},{"orpha":180071,"name":"Unilateral aplasia of the Müllerian ducts","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant"],"onset":["Adolescent","Adult"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"1-5 / 10 000","value":0.0,"area":"Finland","status":"Not yet validated","source":"ORPHANET_11570363[PMID]"},{"type":"Prevalence at birth","qualification":"Value and class","class":"1-5 / 10 000","value":10.0,"area":"Finland","status":"Validated","source":"11570363[PMID]"},{"type":"Point prevalence","qualification":"Class only","class":"1-5 / 10 000","value":0.0,"area":"Europe","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}