{"orpha":93973,"name":"Carpenter-Waziri 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 Alpha-thalassemia-X-linked intellectual disability syndrome","url":"https://raremap.alftech.space/d/ORPHA-93973/","orphanet_url":"https://www.orpha.net/en/disease/detail/93973","names":{"fr":{"name":"Syndrome de Carpenter-Waziri"},"de":{"name":"Carpenter-Waziri-Syndrom"},"es":{"name":"Síndrome de Carpenter-Waziri"},"it":{"name":"Sindrome di Carpenter-Waziri"},"nl":{"name":"Syndroom van Carpenter-Waziri"},"pt":{"name":"Síndrome Carpenter-Waziri"},"pl":{"name":"Zespół Carpentera i Waziri"},"cs":{"name":"Carpenterové-Waziriové syndrom","synonyms":["Carpenter-Waziriové syndrom"]},"uk":{"name":"Синдром Карпентера-Вазірі"},"zh":{"name":"Carpenter-Waziri综合征"},"tr":{"name":"Carpenter-Waziri sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":847,"name":"X-linked alpha-thalassemia-intellectual disability syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}