ICD-10 Diagnosis Code I27.2

Other secondary pulmonary hypertension

Diagnosis Code I27.2

ICD-10: I27.2
Short Description: Other secondary pulmonary hypertension
Long Description: Other secondary pulmonary hypertension
This is the 2017 version of the ICD-10-CM diagnosis code I27.2

Valid for Submission
The code I27.2 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Diseases of the circulatory system (I00–I99)
    • Pulmonary heart disease and diseases of pulmonary circulation (I26-I28)
      • Other pulmonary heart diseases (I27)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code I27.2 is grouped in the following Diagnostic Related Group(s) (MS-DRG v33.0)

  • OTHER CIRCULATORY SYSTEM DIAGNOSES WITH MCC 314
  • OTHER CIRCULATORY SYSTEM DIAGNOSES WITH CC 315
  • OTHER CIRCULATORY SYSTEM DIAGNOSES WITHOUT CC/MCC 316

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

Synonyms
  • Associated pulmonary arterial hypertension
  • Associated pulmonary arterial hypertension
  • Associated pulmonary arterial hypertension
  • Associated pulmonary arterial hypertension
  • Associated pulmonary arterial hypertension
  • Associated pulmonary arterial hypertension
  • Associated pulmonary arterial hypertension
  • Episodic pulmonary hypertension
  • Facultative pulmonary hypertension with shunt at atrial level
  • High altitude pulmonary hypertension
  • Large vessel pulmonary hypertension
  • Portopulmonary hypertension
  • Post-arteritic pulmonary hypertension
  • Post-capillary pulmonary hypertension
  • Post-capillary pulmonary hypertension
  • Post-capillary pulmonary hypertension
  • Progressive pulmonary hypertension
  • Pulmonary arterial hypertension associated with chronic hemolytic anemia
  • Pulmonary arterial hypertension associated with congenital heart disease
  • Pulmonary arterial hypertension associated with congenital systemic-to-pulmonary shunt
  • Pulmonary arterial hypertension associated with connective tissue disease
  • Pulmonary arterial hypertension associated with human immunodeficiency virus infection
  • Pulmonary arterial hypertension associated with schistosomiasis
  • Pulmonary arterial hypertension caused by toxin
  • Pulmonary hypertension
  • Pulmonary hypertension associated with chronic underventilation
  • Pulmonary hypertension associated with chronic underventilation
  • Pulmonary hypertension caused by drug
  • Pulmonary hypertension due to alveolar hypoventilation disorder
  • Pulmonary hypertension due to chronic obstructive pulmonary disease
  • Pulmonary hypertension due to developmental abnormality of the lung
  • Pulmonary hypertension due to diastolic systemic ventricular dysfunction
  • Pulmonary hypertension due to hematological disorder
  • Pulmonary hypertension due to hematological disorder
  • Pulmonary hypertension due to interstitial lung disease
  • Pulmonary hypertension due to left-sided valvular heart disease
  • Pulmonary hypertension due to left-sided valvular heart disease
  • Pulmonary hypertension due to lung disease and/or hypoxia
  • Pulmonary hypertension due to lung disease and/or hypoxia
  • Pulmonary hypertension due to lung disease and/or hypoxia
  • Pulmonary hypertension due to lung disease and/or hypoxia
  • Pulmonary hypertension due to myeloproliferative disorder
  • Pulmonary hypertension due to post-splenectomy hematological disorder
  • Pulmonary hypertension due to pulmonary disease with mixed restrictive and obstructive pattern
  • Pulmonary hypertension due to sleep-disordered breathing
  • Pulmonary hypertension due to systolic systemic ventricular dysfunction
  • Pulmonary hypertension due to vasculitis
  • Pulmonary hypertension in Langerhans cell histiocytosis
  • Pulmonary hypertension in lymphangioleiomyomatosis
  • Pulmonary hypertension in neurofibromatosis
  • Pulmonary hypertension in sarcoidosis
  • Pulmonary hypertension in systemic disorder
  • Pulmonary hypertension in systemic disorder
  • Pulmonary hypertension secondary to raised pulmonary vascular resistance
  • Pulmonary hypertension with extreme obesity
  • Pulmonary hypertension with occult mitral stenosis
  • Pulmonary hypertensive arterial disease
  • Pulmonary hypertensive venous disease
  • Pulmonary lymphangioleiomyomatosis
  • Pulmonary sarcoidosis
  • Pulmonary thrombosis
  • Pulmonary veno-occlusive disease
  • Pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis
  • Pulmonary venous hypertension as complication of procedure
  • Pulmonary venous hypertension due to compression of pulmonary great vein
  • Pulmonary venous hypertension due to compression of pulmonary great vein by lymphadenopathy
  • Pulmonary venous hypertension due to compression of pulmonary great vein by neoplasm
  • Pulmonary venous hypertension due to compression of pulmonary great vein by sclerosing mediastinitis
  • Pulmonary venous hypertension due to congenital stenosis of pulmonary vein
  • Pulmonary venous hypertension due to disorder of left heart
  • Pulmonary venous hypertension due to disorder of left heart
  • Secondary pulmonary hypertension
  • Small vessel pulmonary hypertension
  • Small vessel pulmonary hypertension
  • Solitary pulmonary hypertension
  • Solitary pulmonary hypertension
  • Solitary pulmonary hypertension
  • Thromboembolic pulmonary hypertension

Index of Diseases and Injuries
References found for the code I27.2 in the Index of Diseases and Injuries:


Information for Patients


Pulmonary Hypertension

Also called: Pulmonary arterial hypertension

Pulmonary hypertension (PH) is high blood pressure in the arteries to your lungs. It is a serious condition. If you have it, the blood vessels that carry blood from your heart to your lungs become hard and narrow. Your heart has to work harder to pump the blood through. Over time, your heart weakens and cannot do its job and you can develop heart failure.

Symptoms of PH include

  • Shortness of breath during routine activity, such as climbing two flights of stairs
  • Tiredness
  • Chest pain
  • A racing heartbeat
  • Pain on the upper right side of the abdomen
  • Decreased appetite

As PH worsens, you may find it hard to do any physical activities.

There are two main kinds of PH. One runs in families or appears for no known reason. The other kind is related to another condition, usually heart or lung disease.

There is no cure for PH. Treatments can control symptoms. They involve treating the heart or lung disease, medicines, oxygen, and sometimes lung transplantation.

NIH: National Heart, Lung, and Blood Institute

  • Cor pulmonale
  • Lung diffusion testing
  • Pulmonary angiography
  • Pulmonary hypertension


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