{"orpha":641343,"name":"Imprinting disorders","type":"Clinical group","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-641343/","orphanet_url":"https://www.orpha.net/en/disease/detail/641343","names":{"fr":{"name":"Maladies liées à des anomalies de l'empreinte génétique"},"de":{"name":"Imprintingerkrankung"},"es":{"name":"Trastornos de la impronta"},"it":{"name":"Malattie da alterato imprinting"},"nl":{"name":"Imprintingsstoornissen"},"pt":{"name":"Doenças de imprinting"},"pl":{"name":"Zaburzenia piętnowania"},"cs":{"name":"Poruchy imprintingu"},"uk":{"name":"Порушення імпринтингу"}},"xrefs":[{"source":"MeSH","code":"D000096803","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5816793","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98053,"name":"Rare genetic disease"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":72,"name":"Angelman syndrome","type":"Malformation syndrome"},{"orpha":116,"name":"Beckwith-Wiedemann syndrome","type":"Malformation syndrome"},{"orpha":254519,"name":"Kagami-Ogata syndrome","type":"Malformation syndrome"},{"orpha":739,"name":"Prader-Willi syndrome","type":"Disease"},{"orpha":79443,"name":"Pseudohypoparathyroidism type 1A","type":"Disease"},{"orpha":94089,"name":"Pseudohypoparathyroidism type 1B","type":"Disease"},{"orpha":79444,"name":"Pseudohypoparathyroidism type 1C","type":"Disease"},{"orpha":79445,"name":"Pseudopseudohypoparathyroidism","type":"Disease"},{"orpha":398069,"name":"Schaaf-Yang syndrome","type":"Disease"},{"orpha":813,"name":"Silver-Russell syndrome","type":"Disease"},{"orpha":254516,"name":"Temple syndrome","type":"Malformation syndrome"},{"orpha":99886,"name":"Transient neonatal diabetes mellitus","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}