ICD-10-CM Code E84.8
Cystic fibrosis with other manifestations
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
E84.8 is a billable ICD code used to specify a diagnosis of cystic fibrosis with other manifestations. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E84 is used to code Cystic fibrosis
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs but also the pancreas, liver, kidneys, and intestine. Long-term issues include difficulty breathing and coughing up mucus as a result of frequent lung infections. Other signs and symptoms include sinus infections, poor growth, fatty stool, clubbing of the fingers and toes, and infertility in males among others. Different people may have different degrees of symptoms.
|Specialty:||Medical Genetics, Pulmonology|
|ICD 9 Code:||277.0|
Clubbing in the fingers of a person with cystic fibrosis
- DRG Group #640-641 - Misc disorders of nutrition, metabolism, fluids or electrolytes with MCC.
- DRG Group #640-641 - Misc disorders of nutrition, metabolism, fluids or electrolytes without MCC.
Related Concepts SNOMET-CT
- Pancreatic insufficiency due to cystic fibrosis of pancreas (disorder)
ICD-10-CM Alphabetical Index References for 'E84.8 - Cystic fibrosis with other manifestations'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E84.8. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 277.09 was previously used, E84.8 is the appropriate modern ICD10 code.