{"orpha":2574,"name":"Moynahan syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Alopecia-epilepsy-intellectual disability syndrome, Moynahan type"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Alopecia-intellectual disability syndrome","url":"https://raremap.alftech.space/d/ORPHA-2574/","orphanet_url":"https://www.orpha.net/en/disease/detail/2574","names":{"fr":{"name":"Syndrome de Moynahan","synonyms":["Syndrome d'alopécie-épilepsie-déficience intellectuelle"]},"de":{"name":"Moynahan-Syndrom","synonyms":["Alopezie-Epilepsie-Intelligenzminderung-Syndrom Typ Moynahan"]},"es":{"name":"Síndrome de Moynahan","synonyms":["Síndrome de alopecia-epilepsia-discapacidad intelectual, tipo Moynahan"]},"it":{"name":"Sindrome di Moynahan","synonyms":["Alopecia - epilessia - oligofrenia"]},"nl":{"name":"Syndroom van Moynahan","synonyms":["Alopecie - epilepsie - intellectuele achterstand-syndroom, Moynahan-type"]},"pt":{"name":"Síndrome Moynahan","synonyms":["Síndrome de alopecia-epilepsia-perturbação do desenvolvimento intelectual, tipo Moynahan"]},"pl":{"name":"Zespół Moynahana","synonyms":["Zespół łysienie-padaczka-oligofrenia, typu Moynahana"]},"cs":{"name":"Moynahanův syndrom","synonyms":["Syndrom zahrnující alopecii, epilepsii a oligofrenii, Moynahanův typ"]},"uk":{"name":"Синдром Мойнахена","synonyms":["Синдром алопеції-епілепсії-інтелектуальної недостатності, тип Мойнахана"],"definition":"A rare, genetic, epilepsy syndrome characterized by congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated."},"zh":{"name":"Moynahan综合征","synonyms":["脱发-癫痫-智力障碍综合征，Moynahan型"]},"tr":{"name":"Moynahan sendromu","synonyms":["Alopesi-epilepsi-zihinsel yetersizlik sendromu, Moynahan tipi"]}},"xrefs":[{"source":"OMIM","code":"203600","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"0008755","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C537052","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0265328","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"606","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":2850,"name":"Alopecia-intellectual disability syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}