{"orpha":99142,"name":"Microcephaly-cutis verticis gyrata-lymphedema syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cohen syndrome","url":"https://raremap.alftech.space/d/ORPHA-99142/","orphanet_url":"https://www.orpha.net/en/disease/detail/99142","names":{"fr":{"name":"Syndrome de microcéphalie-cutis verticis gyrata-lymphoedème"},"de":{"name":"Mizrocephalie - Cutis verticis gyrata - Lymphödem"},"es":{"name":"Síndrome de microcefalia-cutis verticis gyrata-linfedema"},"it":{"name":"Microcefalia - cutis verticis gyrata - linfedema"},"nl":{"name":"Microcefalie - cutis verticis gyrata - lymfoedeem"},"pt":{"name":"Síndrome de microcefalia-cutis verticis gyrata-linfedema"},"pl":{"name":"Mikrocefalia - skóra kręta ciemienia - obrzęk limfatyczny"},"cs":{"name":"Syndrom zahrnující mikrocefalii, cutis verticis gyrata a lymfedém"},"uk":{"name":"Синдром мікроцефалії-складчастої пахідермії (cutis vertigus gypata)- лімфедеми"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":193,"name":"Cohen syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}