{"orpha":2355,"name":"Kumar-Levick syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Nail dysplasia-camptodactyly-brachydactyly type B syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cooks syndrome","url":"https://raremap.alftech.space/d/ORPHA-2355/","orphanet_url":"https://www.orpha.net/en/disease/detail/2355","names":{"fr":{"name":"Syndrome de Kumar-Levick","synonyms":["Syndrome de dysplasie des ongles-camptodactylie-brachydactylie type B"]},"de":{"name":"Kumar-Levick-Syndrom","synonyms":["Anonychie - Onychodystrophie - Brachydaktylie Typ B - Ektrodaktylie"]},"es":{"name":"Síndrome de Kumar Levick","synonyms":["Anoniquia-onicodistrofia-braquidactilia tipo B-ectrodactilia"]},"it":{"name":"Sindrome di Kumar-Levick","synonyms":["Displasia ungueale - camptodattilia - brachidattilia tipo B"]},"nl":{"name":"Syndroom van Kumar-Levick","synonyms":["Nageldysplasie - camptodactylie - brachydactylie type B-syndroom"]},"pt":{"name":"Síndrome Kumar-Levick","synonyms":["Síndrome de anoníquia-onicodistrofia-braquidactilia tipo B"]},"pl":{"name":"Zespół Kumara i Levicka","synonyms":["Dysplazja paznokci - kamptodaktylia - brachydaktylia typu B"]},"cs":{"name":"Kumarův-Levickův syndrom","synonyms":["Syndrom zahrnující dysplázii nehtů, kamptodaktylii a brachydaktylii typu B","Kumar-Levickův syndrom"]},"uk":{"name":"Синдром Кумара-Левіка","synonyms":["Синдром дисплазії нігтів-камптодактилія-брахідактилія типу В"]},"zh":{"name":"Kumar-Levick综合征","synonyms":["指甲发育不良-屈曲指-B型短指综合征"]},"tr":{"name":"Kumar-Levick sendromu","synonyms":["Tırnak displazisi-kamptodaktili-brakidaktili tip B sendromu"]}},"xrefs":[{"source":"OMIM","code":"106990","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":1487,"name":"Cooks syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}