{"orpha":98649,"name":"Dentocutaneous 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-98649/","orphanet_url":"https://www.orpha.net/en/disease/detail/98649","names":{"fr":{"name":"Maladie dento-cutanée avec cataracte"},"de":{"name":"Katarakt mit assoziierter dento-kutaner Krankheit"},"es":{"name":"Enfermedad dentocutánea con una posible catarata"},"it":{"name":"Cataratta associata a malattia dentocutanea"},"nl":{"name":"Dentocutane ziekte met cataract"},"pt":{"name":"Doença dentocutânea com catarata"},"pl":{"name":"Anomalie zębowo-skórne z zaćmą"},"cs":{"name":"Dentokutánní onemocnění s kataraktou"},"uk":{"name":"Зубошкірна аномалія з катарактою"},"zh":{"name":"牙皮肤疾病伴白内障"},"tr":{"name":"Katarakt ile seyreden dentokütanöz hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681663","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":1466,"name":"COFS syndrome","type":"Clinical subtype"},{"orpha":627,"name":"Nance-Horan syndrome","type":"Malformation syndrome"},{"orpha":2909,"name":"Rothmund-Thomson syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}