E84.9
BillableCystic fibrosis, unspecified
Cystic fibrosis, unspecified
Coding Notes
Includes
Conditions included under this code
- mucoviscidosis
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Code Also
A second code may be required; sequencing depends on circumstances
- exocrine pancreatic insufficiency (K86.81)
Also Known As / Clinical Terms
SNOMED CT
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Diabetes mellitus associated with pancreatic disease51002006
- Pancreatogenic type 3c diabetes mellitus51002006
- Secondary pancreatic diabetes mellitus51002006
- Cystic fibrosis with no meconium ileus81423003
- Cystic fibrosis without meconium ileus81423003
- CF - Cystic fibrosis190905008
- Cystic fibrosis190905008
- Fibrocystic disease190905008
- Mucoviscidosis190905008
- Cystic fibrosis of pancreas235978006
- Fibrocystic disease of pancreas235978006
- Fibrocystic disease of the pancreas235978006
- Mucoviscidosis of pancreas235978006
- Hamartoma of pilosebaceous apparatus400120004
- Diabetes mellitus due to cystic fibrosis427089005
- Follicular hamartoma with alopecia and cystic fibrosis syndrome716088000
- Classical cystic fibrosis762269004
- Atypical cystic fibrosis762270003
- Subclinical cystic fibrosis762271004
- Cystic fibrosis due to heterozygous deltaF508 mutation1296527009
- DeltaF508 heterozygous cystic fibrosis1296527009
- DeltaF508 heterozygous mucoviscidosis1296527009
- Cystic fibrosis due to homozygous deltaF508 mutation1296528004
- DeltaF508 homozygous cystic fibrosis1296528004
- DeltaF508 homozygous mucoviscidosis1296528004
- Early neonatal jaundice due to mucoviscidosis1335876002
UMLS
- CF - Cystic fibrosisC0010674
- CYSTIC FIBROSISC0010674
- Cystic FibrosisC0010674
- Cystic fibrosisC0010674
- Cystic fibrosis (disorder)C0010674
- Cystic fibrosis NOSC0010674
- Cystic fibrosis, unspecifiedC0010674
- Fibrocystic diseaseC0010674
- Fibrosis, CysticC0010674
- MUCOVISCIDOSISC0010674
- MucoviscidosisC0010674
- cystic disorder fibrosisC0010674
- cystic fibrosisC0010674
- cystic fibrosis (CF)C0010674
- cystic fibrosis pancreasC0010674
- disease fibrocysticC0010674
- disease fibrocystic pancreasC0010674
- diseases fibrocysticC0010674
- fibrocystic diseaseC0010674
- fibrocystic disease of pancreasC0010674
- mucoviscidosisC0010674
- pancreas cystic fibrosisC0010674
Frequently Asked Questions
What is ICD-10 code E84.9?
ICD-10-CM code E84.9 represents "Cystic fibrosis, unspecified". It is a billable/specific code that can be used on a claim.
Is E84.9 a billable code?
Yes, E84.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E84.9 in?
E84.9 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E84.9?
E84.9 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 3 more.
What SNOMED CT codes does E84.9 map to?
E84.9 maps to 14 SNOMED CT concepts: 762270003, 190905008, 762269004, 1296527009, 1296528004, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E84.9?
E84.9 is linked to 1 UMLS Concept Unique Identifier: C0010674. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.