{"orpha":37629,"name":"Neonatal neutropenia","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Severe congenital neutropenia","url":"https://raremap.alftech.space/d/ORPHA-37629/","orphanet_url":"https://www.orpha.net/en/disease/detail/37629","names":{"fr":{"name":"Neutropénie néonatale"},"de":{"name":"Neutropenie, neonatale"},"es":{"name":"Neutropenia neonatal"},"it":{"name":"Neutropenia neonatale"},"nl":{"name":"Neonatale neutropenie"},"pt":{"name":"Neutropenia neonatal"},"pl":{"name":"Neutropenia niemowlęca"},"cs":{"name":"Neonatální neutropenie"},"uk":{"name":"Неонатальна нейтропенія"},"zh":{"name":"新生儿中性粒细胞减少症"},"tr":{"name":"Yenidoğan nötropeni"}},"xrefs":[{"source":"UMLS","code":"C0543693","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10029358","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":42738,"name":"Severe congenital neutropenia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}