ICD-9 Diagnosis Code V83.81

Cystic fibrosis gene car

Diagnosis Code V83.81

ICD-9: V83.81
Short Description: Cystic fibrosis gene car
Long Description: Cystic fibrosis gene carrier
This is the 2014 version of the ICD-9-CM diagnosis code V83.81

Code Classification
  • Supplementary classification of factors influencing health status and contact with health services (E)
    • Genetics (V83-V84)
      • V83 Genetic carrier status

Information for Medical Professionals

Information for Patients

Cystic Fibrosis

Also called: CF

Cystic fibrosis (CF) is an inherited disease of the mucus and sweat glands. It affects mostly your lungs, pancreas, liver, intestines, sinuses and sex organs. CF causes your mucus to be thick and sticky. The mucus clogs the lungs, causing breathing problems and making it easy for bacteria to grow. This can lead to problems such as repeated lung infections and lung damage.

The symptoms and severity of CF vary widely. Some people have serious problems from birth. Others have a milder version of the disease that doesn't show up until they are teens or young adults.

Although there is no cure for CF, treatments have improved greatly in recent years. Until the 1980s, most deaths from CF occurred in children and teenagers. Today, with improved treatments, some people who have CF are living into their forties, fifties, or older.

NIH: National Heart, Lung, and Blood Institute

  • Cystic fibrosis
  • Cystic fibrosis - nutritional considerations
  • How to breathe when you are short of breath
  • Neonatal cystic fibrosis screening
  • Postural drainage
  • Sweat electrolytes test
  • Traveling with breathing problems
  • Using oxygen at home

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