{"orpha":716446,"name":"Rare disorder with progressive vitreoretinopathy disorder as a major feature","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-716446/","orphanet_url":"https://www.orpha.net/en/disease/detail/716446","names":{"fr":{"name":"Maladie rare avec vitreoretinopathie progressive comme manifestation majeure"},"de":{"name":"Seltene Störung mit progredienter Vitreoretinopathie als Hauptmerkmal"},"es":{"name":"Trastorno raro con afectación de vitreorretinopatía progresiva como característica principal"},"it":{"name":"Malattia rara con vitroretinopatia progressiva come caratteristica principale"},"nl":{"name":"Zeldzame aandoening met progressieve vitreoretinopathie als een hoofdkenmerk"},"pt":{"name":"Rare disorder with progressive vitreoretinopathy disorder as a major feature"},"pl":{"name":"Rzadkie zaburzenie z witreopatią jako dominującą cechą"},"cs":{"name":"Rare disorder with progressive vitreoretinopathy disorder as a major feature"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":716438,"name":"Rare progressive vitreoretinopathy","classifications":[156,189]}],"children":[{"orpha":271861,"name":"Hereditary ATTR amyloidosis","type":"Disease"},{"orpha":404473,"name":"Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome","type":"Malformation syndrome"},{"orpha":1571,"name":"Knobloch syndrome","type":"Malformation syndrome"},{"orpha":85194,"name":"Spondylo-ocular syndrome","type":"Malformation syndrome"},{"orpha":828,"name":"Stickler syndrome","type":"Disease"},{"orpha":899,"name":"Walker-Warburg syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}