{"orpha":98733,"name":"Noonan syndrome and Noonan-related syndrome","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-98733/","orphanet_url":"https://www.orpha.net/en/disease/detail/98733","names":{"fr":{"name":"Syndrome de Noonan et syndrome associé"},"de":{"name":"Noonan-Syndrom und Noonan-ähnliches Syndrom"},"es":{"name":"Síndrome de Noonan y síndromes tipo Noonan"},"it":{"name":"Sindrome di Noonan e Noonan-simile"},"nl":{"name":"Syndroom van Noonan en Noonan-gerelateerd syndroom"},"pt":{"name":"Síndrome Noonan e síndrome Noonan-relacionada"},"pl":{"name":"Zespół Noonan i zespoły pokrewne"},"cs":{"name":"Syndrom Noonanové a příbuzné syndromy"},"uk":{"name":"Синдром Нунана та Нунан-повязаний синдром"},"zh":{"name":"努南综合征和努南相关综合征"},"tr":{"name":"Noonan sendromu ve Noonan ilişkili sendrom"}},"xrefs":[{"source":"MONDO","code":"0020297","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681679","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183570,"name":"Genetic malformation syndrome with short stature","classifications":[156]},{"orpha":139021,"name":"Malformation syndrome with short stature","classifications":[147]},{"orpha":536391,"name":"RASopathy","classifications":[156]},{"orpha":156532,"name":"Rare syndrome with cardiac malformations","classifications":[147,148,156]}],"children":[{"orpha":1340,"name":"Cardiofaciocutaneous syndrome","type":"Malformation syndrome"},{"orpha":3071,"name":"Costello syndrome","type":"Malformation syndrome"},{"orpha":638,"name":"Neurofibromatosis-Noonan syndrome","type":"Malformation syndrome"},{"orpha":648,"name":"Noonan syndrome","type":"Malformation syndrome"},{"orpha":500,"name":"Noonan syndrome with multiple lentigines","type":"Malformation syndrome"},{"orpha":363972,"name":"Noonan syndrome-like disorder with juvenile myelomonocytic leukemia","type":"Malformation syndrome"},{"orpha":2701,"name":"Noonan syndrome-like disorder with loose anagen hair","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}