{"orpha":93970,"name":"Holmes-Gang 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-93970/","orphanet_url":"https://www.orpha.net/en/disease/detail/93970","names":{"fr":{"name":"Syndrome de Holmes-Gang"},"de":{"name":"Holmes-Gang-Syndrom"},"es":{"name":"Síndrome de Holmes-Gang"},"it":{"name":"Sindrome di Holmes-Gang"},"nl":{"name":"Syndroom van Holmes-Gang"},"pt":{"name":"Síndrome de Holmes-Gang"},"pl":{"name":"Zespół Holmesa i Ganga"},"cs":{"name":"Holmesův-Gangův syndrom","synonyms":["Holmes-Gangův syndrom"]},"uk":{"name":"Синдром Холмса-Ганга"},"zh":{"name":"Holmes-Gang综合征","definition":"一种X染色体连锁遗传精神发育迟滞（XLMR）综合征，属于以智力缺陷和肌无力面容（智力低下，X染色体连锁遗传-肌无力面容）为特征的一组疾病中的一种。"},"tr":{"name":"Holmes-Gang 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}