{"code":"Q61.2","type":"code","title":"Polycystic kidney, adult type","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["acquired cyst of kidney (N28.1)","Potter's syndrome (Q60.6)"],"excludes2":[],"isBillable":true,"fyEffectivity":{"fy2026":true,"fy2027":true},"sibling_codes":["Q61","Q61.0","Q61.1","Q61.3","Q61.4","Q61.5","Q61.8","Q61.9"],"inclusionTerms":["Polycystic kidney, autosomal dominant"],"sibling_titles":{"code":"Q61.9","title":"Cystic kidney disease, unspecified","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"Polycystic kidney, adult type is a billable ICD-10-CM diagnosis code (Q61.2). Inclusion terms: Polycystic kidney, autosomal dominant. Excludes1 (not coded here): acquired cyst of kidney (N28.1); Potter's syndrome (Q60.6).","officialDefinition":"Polycystic kidney, adult type is a billable ICD-10-CM diagnosis code (Q61.2). Inclusion terms: Polycystic kidney, autosomal dominant. Excludes1 (not coded here): acquired cyst of kidney (N28.1); Potter's syndrome (Q60.6).","seventhCharacterInstructions":[],"workflowProtocols":[],"guidelines":{"whenToUse":[],"whenNotToUse":[],"commonBillingMistakes":[],"codeComparisons":[],"documentationChecklist":[]},"domainLandscape":{"summary":"Primary diagnostic domain and clinical landscape evaluation.","keyCategories":[],"diagnosticContinuum":"Progression continuum from acute presentation to resolution."},"children":[],"hierarchy":[],"relatedCodes":[],"relevantCPTCodes":[],"documentationTips":[],"caseStudies":[],"description":"","overview":""}