Diagnosis Code V83.81
Information for Medical Professionals
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.
- Z14.1 - Cystic fibrosis carrier
Index of Diseases and Injuries
References found for the code V83.81 in the Index of Diseases and Injuries:
- Carrier (suspected) of
- cystic fibrosis gene V83.81
Information for Patients
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