{"code":"Q87.1","type":"code","title":"Congenital malformation syndromes predominantly associated with short stature","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["Ellis-van Creveld syndrome (Q77.6)","Smith-Lemli-Opitz syndrome (E78.72)"],"excludes2":[],"isBillable":false,"fyEffectivity":{"fy2026":true,"fy2027":true},"inclusionTerms":[],"useAdditionalCode":["code(s) to identify all associated manifestations"],"clinicalDefinition":"Congenital malformation syndromes predominantly associated with short stature is a non-billable ICD-10-CM category code (Q87.1). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Ellis-van Creveld syndrome (Q77.6); Smith-Lemli-Opitz syndrome (E78.72). Use additional code: code(s) to identify all associated manifestations.","officialDefinition":"Congenital malformation syndromes predominantly associated with short stature is a non-billable ICD-10-CM category code (Q87.1). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Ellis-van Creveld syndrome (Q77.6); Smith-Lemli-Opitz syndrome (E78.72). Use additional code: code(s) to identify all associated manifestations.","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":""}