{"orpha":139477,"name":"Al-Gazali-Dattani 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 SRD5A3-CDG","url":"https://raremap.alftech.space/d/ORPHA-139477/","orphanet_url":"https://www.orpha.net/en/disease/detail/139477","names":{"fr":{"name":"Syndrome d'Al-Gazali-Dattani"},"de":{"name":"Al-Gazali-Dattani-Syndrom"},"es":{"name":"Síndrome de Al-Gazali-Dattani"},"it":{"name":"Sindrome di Al-Gazali-Dattani"},"nl":{"name":"Syndroom van Al-Gazali-Dattani","synonyms":["CDG1Q"]},"pt":{"name":"Síndrome de Al-Gazali-Dattani"},"pl":{"name":"Zespół Al-Gazaliego i Dattaniego"},"cs":{"name":"Al-Gazaliové-Dattaniho syndrom","synonyms":["Al-Gazali-Dattaniho syndrom"]},"uk":{"name":"Синдром Аль-Газалі-Даттані"},"zh":{"name":"Al-Gazali-Dattani综合征"},"tr":{"name":"Al-Gazali-Dattani sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":324737,"name":"SRD5A3-CDG"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}