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cystic fibrosis

Medical Definition

Most common potentially lethal autosomal recessive disease affecting caucasians; characterized by chronic pulmonary, intestinal, liver, pancreatic, and exocrine gland dysfunction; caused by mutations of the cftr chloride channel.

Wikipedia Summary

Cystic fibrosis (CF) is a genetic disorder inherited in an autosomal recessive manner that impairs the normal clearance of mucus from the lungs, which facilitates the colonization and infection of the lungs by bacteria, notably Staphylococcus aureus. CF is a rare genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine...
Related Codes (8)
Code
Description
Billable
Details
E84Cystic fibrosis
E84.0Cystic fibrosis with pulmonary manifestations
Additional Codes (2)
E84.1Cystic fibrosis with intestinal manifestations
E84.11Meconium ileus in cystic fibrosis
Type 1 Excludes (1)
E84.19Cystic fibrosis with other intestinal manifestations
E84.8Cystic fibrosis with other manifestations
E84.9Cystic fibrosis, unspecified
P09.4Abnormal findings on neonatal screening for cystic fibrosis

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