{"orpha":717585,"name":"Kasabach-Merritt-like phenomenon","type":"Particular clinical situation in a disease or syndrome","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-717585/","orphanet_url":"https://www.orpha.net/en/disease/detail/717585","names":{"fr":{"name":"Phénomène de type Kasabach-Merritt"},"de":{"name":"Kasabach-Merritt-artiges Phänomen"},"es":{"name":"Fenómeno similar al de Kasabach-Merritt"},"it":{"name":"Fenomeno simil-Kasabach-Merritt"},"nl":{"name":"Kasabach-Merritt-achtig fenomeen"},"pt":{"name":"Kasabach-Merritt-like phenomenon"},"pl":{"name":"Zjawisko podobne do Kasabacha-Merritta"},"cs":{"name":"Kasabach-Merritt-like phenomenon"}},"xrefs":[{"source":"ICD-10","code":"P54.8","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"KA8Y","qualifier":"NTBT","icd_relation":"attributed","validated":true,"icd11_uri":"null"}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":717582,"name":"Coagulation abnormality associated with a vascular anomaly","classifications":[147,198]},{"orpha":248308,"name":"Rare hemorrhagic disorder","classifications":[194]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Infancy","Neonatal"],"prevalence":[],"phenotypes":null}