{"orpha":93420,"name":"FGFR3-related chondrodysplasia","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-93420/","orphanet_url":"https://www.orpha.net/en/disease/detail/93420","names":{"fr":{"name":"Chondrodysplasie liée à FGFR3"},"de":{"name":"FGFR3-abhängige Chondrodysplasie"},"es":{"name":"Condrodisplasia asociada a FGFR3"},"it":{"name":"Condroplasia FGFR3-correlata"},"nl":{"name":"FGFR3-gerelateerde chondrodysplasie"},"pt":{"name":"Condrodisplasia FGFR3-relacionada"},"pl":{"name":"Achondroplazja i anomalia FGFR3"},"cs":{"name":"Chondrodysplázie asociované s defektem FGFR3"},"uk":{"name":"Хондродисплазія, повязана з FGFR3"},"zh":{"name":"FGFR3相关软骨发育不全"},"tr":{"name":"FGFR3-ilişkili kondrodisplazi"}},"xrefs":[{"source":"MONDO","code":"0019685","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681604","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":15,"name":"Achondroplasia","type":"Disease"},{"orpha":85164,"name":"Camptodactyly-tall stature-scoliosis-hearing loss syndrome","type":"Disease"},{"orpha":429,"name":"Hypochondroplasia","type":"Disease"},{"orpha":85165,"name":"Severe achondroplasia-developmental delay-acanthosis nigricans syndrome","type":"Disease"},{"orpha":2655,"name":"Thanatophoric dysplasia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Prevalence at birth","qualification":"Value and class","class":"1-9 / 100 000","value":8.1,"area":"United States","status":"Validated","source":"22461456[PMID]"}],"phenotypes":null}