{"code":"Q60.0","type":"code","title":"Renal agenesis, unilateral","codeAlso":[],"includes":["congenital absence of kidney","congenital atrophy of kidney","infantile atrophy of kidney"],"modern_v":"official26","codeFirst":[],"excludes1":[],"excludes2":[],"isBillable":true,"fyEffectivity":{"fy2026":true,"fy2027":true,"billableFy2026":true,"billableFy2027":true},"sibling_codes":["Q60","Q60.1","Q60.2","Q60.3","Q60.4","Q60.5","Q60.6"],"inclusionTerms":[],"sibling_titles":{"code":"Q60.6","title":"Potter's syndrome","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"Renal agenesis, unilateral is a billable ICD-10-CM diagnosis code (Q60.0). Includes: congenital absence of kidney; congenital atrophy of kidney; infantile atrophy of kidney.","officialDefinition":"Renal agenesis, unilateral is a billable ICD-10-CM diagnosis code (Q60.0). Includes: congenital absence of kidney; congenital atrophy of kidney; infantile atrophy of kidney.","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":""}