{"orpha":98610,"name":"Rare disorder with conjunctival involvement 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-98610/","orphanet_url":"https://www.orpha.net/en/disease/detail/98610","names":{"fr":{"name":"Maladie rare avec atteinte conjonctivale comme manifestation majeure"},"de":{"name":"Bindehautkrankheit, seltene"},"es":{"name":"Enfermedad rara de la conjuntiva"},"it":{"name":"Malattia congiuntivale rara"},"nl":{"name":"Zeldzame aandoening met betrokkenheid van conjunctiva als hoofdkenmerk"},"pt":{"name":"Doença rara com envolvimento da conjuntiva como característica principal"},"pl":{"name":"Rzadka choroba spojówki"},"cs":{"name":"Vzácná onemocnění spojivky"},"uk":{"name":"Рідкісний розлад із залученням конюнктиви як основної ознаки"},"zh":{"name":"罕见结膜受累为主要表现疾病"},"tr":{"name":"Esas klinik özelliği konjonktiva tutulumu olan nadir bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681650","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98611,"name":"OBSOLETE: Conjunctival vascular anomaly","status":"inactive"},{"type":"Referred to","orpha":98612,"name":"OBSOLETE: Conjunctival hemangioma or hemolymphangioma","status":"inactive"},{"type":"Referred to","orpha":98613,"name":"OBSOLETE: Conjunctival telangiectasia","status":"inactive"},{"type":"Referred to","orpha":98614,"name":"OBSOLETE: Conjunctival lymphangiectasia","status":"inactive"},{"type":"Referred to","orpha":98615,"name":"OBSOLETE: Pigmented conjunctival lesion","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519284,"name":"Rare disorder of the anterior segment of the eye","classifications":[189]}],"children":[{"orpha":2989,"name":"Familial pterygium of the conjunctiva","type":"Morphological anomaly"},{"orpha":774,"name":"Hereditary hemorrhagic telangiectasia","type":"Disease"},{"orpha":722,"name":"Hypoplasminogenemia","type":"Disease"},{"orpha":2407,"name":"Laryngo-onycho-cutaneous syndrome","type":"Disease"},{"orpha":99922,"name":"Ocular cicatricial pemphigoid","type":"Disease"},{"orpha":519280,"name":"Rare conjunctivitis","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}