{"code":"G71.0340","type":"code","title":"Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":[],"excludes2":["arthrogryposis multiplex congenita (Q74.3)","metabolic disorders (E70-E88)","myositis (M60.-)"],"isBillable":true,"fyEffectivity":{"fy2026":true,"fy2027":true,"billableFy2026":true,"billableFy2027":true},"inclusionTerms":["Sarcoglycanopathy, NOS"],"useAdditionalCode":[],"clinicalDefinition":"Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified is a billable ICD-10-CM diagnosis code (G71.0340). Inclusion terms: Sarcoglycanopathy, NOS. Excludes2 (not included here): arthrogryposis multiplex congenita (Q74.3); metabolic disorders (E70-E88); myositis (M60.-).","officialDefinition":"Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified is a billable ICD-10-CM diagnosis code (G71.0340). Inclusion terms: Sarcoglycanopathy, NOS. Excludes2 (not included here): arthrogryposis multiplex congenita (Q74.3); metabolic disorders (E70-E88); myositis (M60.-).","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":{"arthrogryposis multiplex congenita (Q74.3)":"G71","metabolic disorders (E70-E88)":"G71","myositis (M60.-)":"G71"},"hcc":{"mapped":true,"model":"CMS-HCC V28","paymentYear":"2026","categories":[{"hcc":"197","label":"Muscular Dystrophy","family":"","suppresses":[]}],"otherModels":[{"model":"CMS-HCC V22","hcc":"76"}]}}