{"code":"Q61.1","type":"code","title":"Polycystic kidney, infantile type","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["acquired cyst of kidney (N28.1)","Potter's syndrome (Q60.6)"],"excludes2":[],"isBillable":false,"fyEffectivity":{"fy2026":true,"fy2027":true,"billableFy2026":false,"billableFy2027":false},"inclusionTerms":["Polycystic kidney, autosomal recessive"],"useAdditionalCode":[],"clinicalDefinition":"Polycystic kidney, infantile type is a non-billable ICD-10-CM category code (Q61.1). A more specific billable subcode must be selected for claims submission. Inclusion terms: Polycystic kidney, autosomal recessive. Excludes1 (not coded here): acquired cyst of kidney (N28.1); Potter's syndrome (Q60.6).","officialDefinition":"Polycystic kidney, infantile type is a non-billable ICD-10-CM category code (Q61.1). A more specific billable subcode must be selected for claims submission. Inclusion terms: Polycystic kidney, autosomal recessive. 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":"","noteProvenance":{"acquired cyst of kidney (N28.1)":"Q61","Potter's syndrome (Q60.6)":"Q61"},"hcc":{"mapped":false,"model":"CMS-HCC V28","paymentYear":"2026","categories":[],"otherModels":[]}}