{"code":"Q82.8","type":"code","title":"Other specified congenital malformations of skin","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["Ehlers-Danlos syndromes (Q79.6-)","acrodermatitis enteropathica (E83.2)","congenital erythropoietic porphyria (E80.0)","pilonidal cyst or sinus (L05.-)","Sturge-Weber (-Dimitri) syndrome (Q85.89)"],"excludes2":["disorders of pyrophosphate metabolism (E83.82-)"],"isBillable":true,"fyEffectivity":{"fy2026":true,"fy2027":true,"billableFy2026":true,"billableFy2027":true},"sibling_codes":["Q82","Q82.0","Q82.1","Q82.2","Q82.3","Q82.4","Q82.5","Q82.6","Q82.9"],"inclusionTerms":["Abnormal palmar creases","Accessory skin tags","Benign familial pemphigus [Hailey-Hailey]","Congenital poikiloderma","Cutis laxa (hyperelastica)","Dermatoglyphic anomalies","Inherited keratosis palmaris et plantaris","Keratosis follicularis [Darier-White]"],"sibling_titles":{"code":"Q82.9","title":"Congenital malformation of skin, unspecified","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"","officialDefinition":"","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":""}