{"orpha":180766,"name":"Malformative syndrome with dentinogenesis imperfecta","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-180766/","orphanet_url":"https://www.orpha.net/en/disease/detail/180766","names":{"fr":{"name":"Syndrome malformatif avec dentinogenèse imparfaite"},"de":{"name":"Fehlbildungssyndrom mit Dentinogenesis imperfecta"},"es":{"name":"Síndrome malformativo con dentinogénesis imperfecta"},"it":{"name":"Sindrome malformativa con dentinogenesi imperfetta"},"nl":{"name":"Malformatief syndroom met dentinogenesis imperfecta"},"pt":{"name":"Síndrome malformativo com dentinogénese imperfeita"},"pl":{"name":"Zespół wad wrodzonych z dentinogenesis imperfecta"},"cs":{"name":"Malformační syndrom s dentinogenesis imperfecta"},"uk":{"name":"Мальформативний синдром з недосконалим дентиногенезом"},"zh":{"name":"伴牙本质发育不全的畸形综合征"},"tr":{"name":"Dentinogenesis imperfekta ile seyreden malformatif sendrom"}},"xrefs":[{"source":"MONDO","code":"15877","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680472","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":139042,"name":"Malformation syndrome with odontal and/or periodontal component","classifications":[147,197]},{"orpha":77830,"name":"Rare genetic odontologic disease","classifications":[156]}],"children":[{"orpha":71267,"name":"Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome","type":"Malformation syndrome"},{"orpha":166272,"name":"Odontochondrodysplasia","type":"Malformation syndrome"},{"orpha":1830,"name":"Schimke immuno-osseous dysplasia","type":"Disease"},{"orpha":166277,"name":"Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}