{"orpha":93423,"name":"Sulfation-related bone disorder","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-93423/","orphanet_url":"https://www.orpha.net/en/disease/detail/93423","names":{"fr":{"name":"Maladie osseuse liée à la sulfatation"},"de":{"name":"Knochenkrankheit bei Sulfatierungsstörung"},"es":{"name":"Trastorno óseo asociado a la sulfatación"},"it":{"name":"Difetto osseo legato alla sulfazione"},"nl":{"name":"Sulfatatiegerelateerde botaandoening"},"pt":{"name":"Doença da sulfatação"},"pl":{"name":"Zaburzenia sulfatyzacji"},"cs":{"name":"Onemocnění kostí související se sulfatací"},"uk":{"name":"Розлади кісток, повязані з сульфатацією"},"zh":{"name":"硫酸化相关骨病"},"tr":{"name":"Sülfasyon-ilişkili kemik bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681607","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":364803,"name":"Rare bone disease related to a common gene or pathway defect","classifications":[156]}],"children":[{"orpha":93298,"name":"Achondrogenesis type 1B","type":"Clinical subtype"},{"orpha":56304,"name":"Atelosteogenesis type II","type":"Malformation syndrome"},{"orpha":628,"name":"Diastrophic dysplasia","type":"Disease"},{"orpha":93307,"name":"Multiple epiphyseal dysplasia type 4","type":"Disease"},{"orpha":93282,"name":"Spondyloepimetaphyseal dysplasia, PAPSS2 type","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}