{"orpha":163637,"name":"Rare disorder related with pregnancy, childbirth and puerperium","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-163637/","orphanet_url":"https://www.orpha.net/en/disease/detail/163637","names":{"fr":{"name":"Maladie rare liée à la grossesse et à la périnatalité"},"de":{"name":"Seltene Krankheit in Verbindung mit Schwangerschaft, Geburt und Wochenbett"},"es":{"name":"Trastornos raros relacionados con embarazo, nacimiento y puerperio"},"it":{"name":"Malattia rara associata a gravidanza, parto e puerperio"},"nl":{"name":"Zeldzame stoornis gerelateerd aan zwangerschap, bevalling en kraambedperiode"},"pt":{"name":"Doença rara relacionada com gravidez, parto e puerpério"},"pl":{"name":"Rzadkie schorzenie związane z ciążą, porodem lub połogiem"},"cs":{"name":"Vzácná onemocnění související s těhotenstvím, porodem a šestinedělím"},"uk":{"name":"Рідкісний розлад, повязаний з вагітністю, пологами та післяпологовим періодом"},"zh":{"name":"妊娠、分娩和产褥期相关罕见疾病"},"tr":{"name":"Gebelik, doğum ve lohusalık ilişkili nadir bozukluk"}},"xrefs":[{"source":"MONDO","code":"15582","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680447","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":96344,"name":"Rare gynecologic or obstetric disease"},"parents":[{"orpha":96344,"name":"Rare gynecologic or obstetric disease","classifications":[205]}],"children":[{"orpha":243367,"name":"Acute fatty liver of pregnancy","type":"Disease"},{"orpha":617304,"name":"Amniotic fluid embolism","type":"Disease"},{"orpha":80,"name":"Antiphospholipid syndrome","type":"Disease"},{"orpha":91,"name":"Aromatase deficiency","type":"Disease"},{"orpha":615970,"name":"Chronic intervillositis of unknown etiology","type":"Disease"},{"orpha":99819,"name":"Familial gestational hyperthyroidism","type":"Disease"},{"orpha":244242,"name":"HELLP syndrome","type":"Disease"},{"orpha":88660,"name":"Hypertension due to gain-of-function mutations in the mineralocorticoid receptor","type":"Disease"},{"orpha":647823,"name":"Idiopathic pregnancy-associated osteoporosis","type":"Disease"},{"orpha":69665,"name":"Intrahepatic cholestasis of pregnancy","type":"Disease"},{"orpha":289385,"name":"Malignancy diagnosed during pregnancy","type":"Particular clinical situation in a disease or syndrome"},{"orpha":563,"name":"Peripartum cardiomyopathy","type":"Disease"},{"orpha":662721,"name":"Placenta accreta spectrum disorder","type":"Disease"},{"orpha":439167,"name":"Placental insufficiency","type":"Clinical syndrome"},{"orpha":443173,"name":"Postpartum psychosis","type":"Disease"},{"orpha":275555,"name":"Preeclampsia","type":"Disease"},{"orpha":723290,"name":"Pregnancy-associated spontaneous coronary artery dissection","type":"Disease"},{"orpha":64745,"name":"Pruritic urticarial papules and plaques of pregnancy","type":"Disease"},{"orpha":617307,"name":"Rare disorder related to monochorionic twin pregnancy","type":"Category"},{"orpha":662786,"name":"Vasa previa","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}