{"query":"mos 47,XY,+21[12]/46,XY[8]","kind":"canonical","recognisedAs":"Variant ID","results":[{"kind":"aneuploidy","id":"trisomy-21-mosaic","route":"/aneuploidy/trisomy-21-mosaic/","label":"trisomy-21-mosaic","description":"Trisomy 21 (mosaic) · from ISCN karyotype"}],"semantic":{"query":"mos 47,XY,+21[12]/46,XY[8]","isNaturalLanguage":true,"matchedPhenotypes":[],"candidateGenes":[],"clinicalReasoning":"No direct clinical phenotype features detected for \"mos 47,XY,+21[12]/46,XY[8]\". Try clinical terms such as \"recurrent seizures\", \"ataxia\", \"microcephaly\", or \"hepatosplenomegaly\".","suggestedTargets":[]}}