{"orpha":181402,"name":"Syndrome with hypoparathyroidism","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-181402/","orphanet_url":"https://www.orpha.net/en/disease/detail/181402","names":{"fr":{"name":"Syndrome avec hypoparathyroïdie"},"de":{"name":"Syndrom mit Hypoparathyreoidismus"},"es":{"name":"Síndrome con hipoparatiroidismo"},"it":{"name":"Malattia associata ad ipoparatiroidismo"},"nl":{"name":"Syndroom met hypoparathyreoïdie"},"pt":{"name":"Síndrome com hipoparatiroidismo"},"pl":{"name":"Zespół z niedoczynnością przytarczyc"},"cs":{"name":"Syndromy s hypoparatyreoidismem"},"uk":{"name":"Синдром гіпопаратиреозу"},"zh":{"name":"伴甲状旁腺功能减退的综合征"},"tr":{"name":"Hipoparatiroidi ile seyreden sendrom"}},"xrefs":[{"source":"MONDO","code":"15895","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680611","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":208593,"name":"Genetic hypoparathyroidism","classifications":[156]},{"orpha":181405,"name":"Rare hypoparathyroidism","classifications":[193]}],"children":[{"orpha":567,"name":"22q11.2 deletion syndrome","type":"Malformation syndrome"},{"orpha":589856,"name":"Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome","type":"Malformation syndrome"},{"orpha":1563,"name":"Dahlberg-Borer-Newcomer syndrome","type":"Malformation syndrome"},{"orpha":2237,"name":"Hypoparathyroidism-sensorineural deafness-renal disease syndrome","type":"Malformation syndrome"},{"orpha":480,"name":"Kearns-Sayre syndrome","type":"Disease"},{"orpha":2333,"name":"Kenny-Caffey syndrome","type":"Malformation syndrome"},{"orpha":5,"name":"Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":699,"name":"Pearson syndrome","type":"Disease"},{"orpha":2323,"name":"Sanjad-Sakati syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}