{"orpha":723156,"name":"Fetal acetylcholine receptor antibody-related disorder","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["FARAD"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-723156/","orphanet_url":"https://www.orpha.net/en/disease/detail/723156","names":{"fr":{"name":"Trouble lié aux anticorps anti-récepteurs de l'acétylcholine foetaux","synonyms":["FARAD"]},"de":{"name":"Fetale Acetylcholinrezeptor-Antikörper-Störung","synonyms":["FARAD","Fetales AChR-Inaktivierungs-Syndrom","FARIS"]},"es":{"name":"Trastorno fetal asociado a anticuerpos receptores de acetilcolina","synonyms":["FARAD"]},"it":{"name":"Malattia correlata agli anticorpi fetali diretti contro il recettore dell'acetilcolina","synonyms":["FARAD"]},"nl":{"name":"Foetale aandoening gerelateerd aan acetylcholinereceptor-antilichaam","synonyms":["FARAD"]},"pt":{"name":"Fetal acetylcholine receptor antibody-related disorder"},"pl":{"name":"Fetal acetylcholine receptor antibody-related disorder","synonyms":["FARAD"]},"cs":{"name":"Fetal acetylcholine receptor antibody-related disorder","synonyms":["FARAD"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":109007,"name":"Arthrogryposis syndrome","classifications":[147]},{"orpha":251535,"name":"Maternal disease-related embryofetopathy","classifications":[147,216]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Antenatal"],"prevalence":[{"type":"Cases/families","qualification":"Case(s)","class":null,"value":46.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"},{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}