{"orpha":98648,"name":"Musculoskeletal disease with cataract","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-98648/","orphanet_url":"https://www.orpha.net/en/disease/detail/98648","names":{"fr":{"name":"Maladie musculo-squelettique avec cataracte"},"de":{"name":"Muskuloskelettale Krankheit mit Katarakt"},"es":{"name":"Enfermedad musculoesquelética con una posible catarata"},"it":{"name":"Cataratta associata a malattia muscoloscheletrica"},"nl":{"name":"Musculoskeletale ziekte met cataract"},"pt":{"name":"Doença musculoesquelética com catarata"},"pl":{"name":"Choroba mięśniowo-szkieletowa z zaćmą"},"cs":{"name":"Muskuloskeletální onemocnění s kataraktou"},"uk":{"name":"Захворювання опорно-рухового апарату з катарактою"},"zh":{"name":"肌肉骨骼疾病伴白内障"},"tr":{"name":"Katarakt ile seyreden kas-iskelet sistemi hastalığı"}},"xrefs":[{"source":"UMLS","code":"C5681664","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98641,"name":"Syndromic cataract","classifications":[189]},{"orpha":522548,"name":"Syndromic genetic cataract","classifications":[156]}],"children":[{"orpha":177,"name":"Rhizomelic chondrodysplasia punctata","type":"Disease"},{"orpha":3103,"name":"Roberts syndrome","type":"Malformation syndrome"},{"orpha":273,"name":"Steinert myotonic dystrophy","type":"Disease"},{"orpha":90653,"name":"Stickler syndrome type 1","type":"Clinical subtype"},{"orpha":90654,"name":"Stickler syndrome type 2","type":"Clinical subtype"},{"orpha":35173,"name":"X-linked dominant chondrodysplasia punctata","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}