{"orpha":171836,"name":"Amelogenesis imperfecta-gingival hyperplasia syndrome","type":"Disease","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 Enamel-renal syndrome","url":"https://raremap.alftech.space/d/ORPHA-171836/","orphanet_url":"https://www.orpha.net/en/disease/detail/171836","names":{"fr":{"name":"Syndrome d'amélogenèse imparfaite-hyperplasie gingivale"},"de":{"name":"Amelogenesis imperfecta-Zahnfleischhyperplasie-Syndrom","synonyms":["Amelogenesis imperfecta-Gingivahyperplasie-Syndrom"]},"es":{"name":"Síndrome de amelogénesis imperfecta-hiperplasia gingival"},"it":{"name":"Sindrome amelogenesi imperfetta-iperplasia gengivale"},"nl":{"name":"Amelogenesis imperfecta - gingivale hyperplasie-syndroom","synonyms":["Amelogenesis imperfecta - tandvleeshyperplasie-syndroom"]},"pt":{"name":"Fibromatose gengival - anomalias dentárias"},"pl":{"name":"Zespół wrodzonego niedorozwoju szkliwa i hiperplazji dziąseł"},"cs":{"name":"Syndrom zahrnující amelogenesis imperfecta a hyperplázii dásní"},"uk":{"name":"Синдром недосконалого амелогенезу - гіперплазія ясен"},"zh":{"name":"釉质发育不全-牙龈增生综合征"},"tr":{"name":"Amelogenezis imperfekta-gingival hiperplazi sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":1031,"name":"Enamel-renal syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}