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ICD-10-CM Codes
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E00-E89
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E70-E88
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E84-
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2023 ICD-10-CM Diagnosis Code E84
2023 ICD-10-CM Diagnosis Code E84
Cystic fibrosis
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
- E84 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- The 2023 edition of ICD-10-CM E84 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E84 - other international versions of ICD-10 E84 may differ.
Code AlsoCode Also Help
A code also note instructs that 2 codes may be required to fully describe a condition but the sequencing of the two codes is discretionary, depending on the severity of the conditions and the reason for the encounter.
IncludesIncludes Help
"Includes" further defines, or give examples of, the content of the code or category.
The following code(s) above
E84 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
E84:
Clinical Information
- A common hereditary disease in which exocrine (secretory) glands produce abnormally thick mucus. This mucus can cause problems in digestion, breathing, and body cooling.
- A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi). The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather.
- An autosomal recessive genetic disease of the exocrine glands. It is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator expressed in several organs including the lung, the pancreas, the biliary system, and the sweat glands. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in airway obstruction; chronic respiratory infections; pancreatic insufficiency; maldigestion; salt depletion; and heat prostration.
- 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.
- 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.
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to E84:
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Code Also: Z71.87
ICD-10-CM Diagnosis Code Z71.87
Encounter for pediatric-to-adult transition counseling
2023 - New Code Billable/Specific Code POA Exempt
Code Also- chronic condition, if applicable, such as:
- autism spectrum disorder (F84.0)
- congenital malformations of the circulatory system (Q20-Q28)
- cystic fibrosis (E84-)
- sickle-cell disorder (D57-)
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Code First: E08, Q55.3, J93.12
ICD-10-CM Diagnosis Code E08
Diabetes mellitus due to underlying condition
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
Code First- the underlying condition, such as:
- congenital rubella (P35.0)
- Cushing's syndrome (E24.-)
- cystic fibrosis (E84.-)
- malignant neoplasm (C00-C96)
- malnutrition (E40-E46)
- pancreatitis and other diseases of the pancreas (K85-K86.-)
Type 1 Excludes- drug or chemical induced diabetes mellitus (E09.-)
- gestational diabetes (O24.4-)
- neonatal diabetes mellitus (P70.2)
- postpancreatectomy diabetes mellitus (E13.-)
- postprocedural diabetes mellitus (E13.-)
- secondary diabetes mellitus NEC (E13.-)
- type 1 diabetes mellitus (E10.-)
- type 2 diabetes mellitus (E11.-)
Use Additional- code to identify control using:
- insulin (Z79.4)
- oral antidiabetic drugs (Z79.84)
- oral hypoglycemic drugs (Z79.84)
ICD-10-CM Diagnosis Code Q55.3
Atresia of vas deferens
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Male Dx POA Exempt
Code First- any associated cystic fibrosis (E84.-)
ICD-10-CM Diagnosis Code J93.12
Secondary spontaneous pneumothorax
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Code First- underlying condition, such as:
- catamenial pneumothorax due to endometriosis (N80.B-)
- cystic fibrosis (E84.-)
- eosinophilic pneumonia (J82)
- lymphangioleiomyomatosis (J84.81)
- malignant neoplasm of bronchus and lung (C34.-)
- Marfan's syndrome (Q87.4)
- pneumonia due to Pneumocystis carinii (B59)
- secondary malignant neoplasm of lung (C78.0-)
- spontaneous rupture of the esophagus (K22.3)
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Type 1 Excludes: Q45.3
ICD-10-CM Diagnosis Code Q45.3
Other congenital malformations of pancreas and pancreatic duct
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
Applicable To- Accessory pancreas
- Congenital malformation of pancreas or pancreatic duct NOS
Type 1 Excludes- congenital diabetes mellitus (E10.-)
- cystic fibrosis (E84.0-E84.9)
- fibrocystic disease of pancreas (E84.-)
- neonatal diabetes mellitus (P70.2)
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Type 2 Excludes: K86
ICD-10-CM Diagnosis Code K86
Other diseases of pancreas
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
Type 2 Excludes- fibrocystic disease of pancreas (E84.-)
- islet cell tumor (of pancreas) (D13.7)
- pancreatic steatorrhea (K90.3)
ICD-10-CM Codes Adjacent To E84
E83.49 Other disorders of magnesium metabolism
E83.5 Disorders of calcium metabolism
E83.50 Unspecified disorder of calcium metabolism
E83.59 Other disorders of calcium metabolism
E83.8 Other disorders of mineral metabolism
E83.89 Other disorders of mineral metabolism
E83.9 Disorder of mineral metabolism, unspecified
E84
Cystic fibrosis
E84.0 Cystic fibrosis with pulmonary manifestations
E84.1 Cystic fibrosis with intestinal manifestations
E84.11 Meconium ileus in cystic fibrosis
E84.19 Cystic fibrosis with other intestinal manifestations
E84.8 Cystic fibrosis with other manifestations
E84.9 Cystic fibrosis, unspecified
E85.0 Non-neuropathic heredofamilial amyloidosis
E85.1 Neuropathic heredofamilial amyloidosis
E85.2 Heredofamilial amyloidosis, unspecified
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.