Chronic Obstructive Pulmonary Disease, Interstitial Lung Disorders, and Other Chronic Lung Disorders
Under the CMS-HCC V28 risk adjustment model (PY2026 Medicare Advantage), HCC 280 carries a community non-dual aged RAF of 0.319, and 79 payable ICD-10-CM diagnosis codes map to it. In the V28 hierarchy it is superseded by HCC 276, HCC 277, HCC 278, HCC 279 when a more severe category in the same disease group is also present.
RAF factors
The community factor varies by Medicaid and originally-disabled status; the institutional factor applies to long-term-institutional members. These are the CMS-HCC V28 PY2026 relative factors.
V28 hierarchy
Trumped by: HCC 276, HCC 277, HCC 278, HCC 279 (a more severe category in the same disease group supersedes this one).
ICD-10-CM codes that map to HCC 280 (79)
Payable diagnosis codes that map to this category under CMS-HCC V28 PY2026. Open any code for its full description, HCC mapping, and coding guidance.
- B44.81Allergic bronchopulmonary aspergillosis
- J41.0Simple chronic bronchitis
- J41.1Mucopurulent chronic bronchitis
- J41.8Mixed simple and mucopurulent chronic bronchitis
- J42Unspecified chronic bronchitis
- J43.0Unilateral pulmonary emphysema [MacLeod's syndrome]
- J43.1Panlobular emphysema
- J43.2Centrilobular emphysema
- J43.8Other emphysema
- J43.9Emphysema, unspecified
- J44.0Chronic obstructive pulmonary disease with (acute) lower respiratory infection
- J44.1Chronic obstructive pulmonary disease with (acute) exacerbation
- J44.81Bronchiolitis obliterans and bronchiolitis obliterans syndrome
- J44.89Other specified chronic obstructive pulmonary disease
- J44.9Chronic obstructive pulmonary disease, unspecified
- J47.0Bronchiectasis with acute lower respiratory infection
- J47.1Bronchiectasis with (acute) exacerbation
- J47.9Bronchiectasis, uncomplicated
- J60Coalworker's pneumoconiosis
- J61Pneumoconiosis due to asbestos and other mineral fibers
- J62.0Pneumoconiosis due to talc dust
- J62.8Pneumoconiosis due to other dust containing silica
- J63.0Aluminosis (of lung)
- J63.1Bauxite fibrosis (of lung)
- J63.2Berylliosis
- J63.3Graphite fibrosis (of lung)
- J63.4Siderosis
- J63.5Stannosis
- J63.6Pneumoconiosis due to other specified inorganic dusts
- J64Unspecified pneumoconiosis
- J65Pneumoconiosis associated with tuberculosis
- J66.0Byssinosis
- J66.1Flax-dressers' disease
- J66.2Cannabinosis
- J66.8Airway disease due to other specific organic dusts
- J67.0Farmer's lung
- J67.1Bagassosis
- J67.2Bird fancier's lung
- J67.3Suberosis
- J67.4Maltworker's lung
- J67.5Mushroom-worker's lung
- J67.6Maple-bark-stripper's lung
- J67.7Air conditioner and humidifier lung
- J67.8Hypersensitivity pneumonitis due to other organic dusts
- J67.9Hypersensitivity pneumonitis due to unspecified organic dust
- J68.0Bronchitis and pneumonitis due to chemicals, gases, fumes and vapors
- J68.1Pulmonary edema due to chemicals, gases, fumes and vapors
- J68.2Upper respiratory inflammation due to chemicals, gases, fumes and vapors, not elsewhere classified
- J68.3Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors
- J68.4Chronic respiratory conditions due to chemicals, gases, fumes and vapors
- J68.8Other respiratory conditions due to chemicals, gases, fumes and vapors
- J68.9Unspecified respiratory condition due to chemicals, gases, fumes and vapors
- J82.81Chronic eosinophilic pneumonia
- J84.01Alveolar proteinosis
- J84.02Pulmonary alveolar microlithiasis
- J84.03Idiopathic pulmonary hemosiderosis
- J84.09Other alveolar and parieto-alveolar conditions
- J84.10Pulmonary fibrosis, unspecified
- J84.111Idiopathic interstitial pneumonia, not otherwise specified
- J84.113Idiopathic non-specific interstitial pneumonitis
- J84.114Acute interstitial pneumonitis
- J84.115Respiratory bronchiolitis interstitial lung disease
- J84.116Cryptogenic organizing pneumonia
- J84.117Desquamative interstitial pneumonia
- J84.178Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
- J84.2Lymphoid interstitial pneumonia
- J84.81Lymphangioleiomyomatosis
- J84.82Adult pulmonary Langerhans cell histiocytosis
- J84.89Other specified interstitial pulmonary diseases
- J84.9Interstitial pulmonary disease, unspecified
- J98.2Interstitial emphysema
- J98.3Compensatory emphysema
- J99Respiratory disorders in diseases classified elsewhere
- M32.13Lung involvement in systemic lupus erythematosus
- M33.01Juvenile dermatomyositis with respiratory involvement
- M33.11Other dermatomyositis with respiratory involvement
- M33.21Polymyositis with respiratory involvement
- M33.91Dermatopolymyositis, unspecified with respiratory involvement
- M35.02Sjogren syndrome with lung involvement
Frequently asked questions
What is CMS-HCC V28 category 280?
HCC 280 is "Chronic Obstructive Pulmonary Disease, Interstitial Lung Disorders, and Other Chronic Lung Disorders", a payment Hierarchical Condition Category in the CMS-HCC V28 risk adjustment model (100% phase-in for payment year 2026). 79 payable ICD-10-CM codes map to it.
What is the RAF weight for HCC 280?
The community non-dual aged relative factor for CMS-HCC V28 category 280 is 0.319. The exact factor varies by enrollment segment (community Medicaid and originally-disabled status, and institutional); the full segment table is published in the CMS V28 Rate Announcement.
How many ICD-10-CM codes map to HCC 280?
79 payable ICD-10-CM diagnosis codes map to CMS-HCC V28 category 280 (Chronic Obstructive Pulmonary Disease, Interstitial Lung Disorders, and Other Chronic Lung Disorders) for payment year 2026.
Which categories trump HCC 280 in the V28 hierarchy?
HCC 280 is superseded by HCC 276 (Lung Transplant Status/Complications), HCC 277 (Cystic Fibrosis), HCC 278 (Idiopathic Pulmonary Fibrosis and Lung Involvement in Systemic Sclerosis), HCC 279 (Severe Persistent Asthma). When a more severe category in the same disease group is documented, it is counted instead of HCC 280.
Source: CMS published ICD-10-CM mapping file plus CMS-HCC v28 PY2026 model software.