{"orpha":137653,"name":"Microcephaly-digital anomalies-intellectual disability syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Kelly-Kirson-Wyatt syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Jawad syndrome","url":"https://raremap.alftech.space/d/ORPHA-137653/","orphanet_url":"https://www.orpha.net/en/disease/detail/137653","names":{"fr":{"name":"Syndrome de microcéphalie-anomalies digitales-déficience intellectuelle","synonyms":["Syndrome de Kelly-Kirson-Wyatt"]},"de":{"name":"Mikrozephalie-digitale Anomalien-Intelligenzminderung-Syndrom","synonyms":["Kelly-Kirson-Wyatt-Syndrom"]},"es":{"name":"Síndrome de microcefalia-anomalías digitales-discapacidad intelectual","synonyms":["Síndrome de Kelly-Kirson-Wyatt"]},"it":{"name":"Sindrome microcefalia-anomalie digitali-deficit cognitivo","synonyms":["Sindrome di Kelly-Kirson-Wyatt"]},"nl":{"name":"Microcefalie - vingeranomalieën - intellectuele achterstand-syndroom","synonyms":["Syndroom van Kelly-Kirson-Wyatt"]},"pt":{"name":"Síndrome de microcefalia-anomalias digitais-perturbação do desenvolvimento intelectual","synonyms":["Síndrome Kelly-Kirson-Wyatt"]},"pl":{"name":"Małogłowie - wady palców - niepełnosprawność intelektualna","synonyms":["Zespół Kelly'ego, Kirsona i Wyatta"]},"cs":{"name":"Syndrom zahrnující mikrocefalii, anomálie prstů a mentální retardaci","synonyms":["Kellyho-Kirsonův-Wyattův syndrom","Kelly-Kirson-Wyattův syndrom"]},"uk":{"name":"Синдром мікроцефалії-аномалії пальців-інтелектуальної недостатності","synonyms":["Синдром Келлі-Кірсона-Вайєтта"]},"zh":{"name":"小头畸形-指异常-智力障碍综合征","synonyms":["Kelly-Kirson-Wyatt综合征"]},"tr":{"name":"Mikrosefali-dijital anomaliler-zihinsel yetersizlik sendromu","synonyms":["Kelly-Kirson-Wyatt sendromu"]}},"xrefs":[],"associations":[{"type":"Moved to","orpha":313795,"name":"Jawad syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}