{"orpha":96344,"name":"Rare gynecologic or obstetric disease","type":"Category","group":"Group of disorders","status":"active","flags":["Head of classification"],"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-96344/","orphanet_url":"https://www.orpha.net/en/disease/detail/96344","names":{"fr":{"name":"Maladie gynécologique ou obstétrique rare"},"de":{"name":"Seltene gynäkologische oder geburtshilfliche Krankheit"},"es":{"name":"Enfermedad ginecológica y obstétrica rara"},"it":{"name":"Malattia ginecologica e ostetrica rara"},"nl":{"name":"Zeldzame gynaecologische of obstetrische ziekte"},"pt":{"name":"Doença ginecológica ou obstétrica rara"},"pl":{"name":"Rzadka choroba ginekologiczna lub położnicza"},"cs":{"name":"Vzácná gynekologicko-porodnická onemocnění"},"uk":{"name":"Рідкісне гінекологічне або акушерське захворювання"},"zh":{"name":"罕见妇产科疾病"},"tr":{"name":"Nadir görülen jinekolojik veya obstetrik hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681537","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[{"orpha":180208,"name":"Anomaly of puberty or/and menstrual cycle","type":"Category"},{"orpha":325620,"name":"Difference of sex development of gynecological interest","type":"Category"},{"orpha":180163,"name":"Rare breast malformation","type":"Category"},{"orpha":163637,"name":"Rare disorder related with pregnancy, childbirth and puerperium","type":"Category"},{"orpha":98063,"name":"Rare gynecological tumor","type":"Category"},{"orpha":180199,"name":"Rare non-malformative gynecologic or obstetric disease","type":"Category"},{"orpha":180151,"name":"Rare vaginal malformation","type":"Category"},{"orpha":180062,"name":"Uterovaginal malformation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}