E84.8
BillableCystic fibrosis with other manifestations
Cystic fibrosis with other manifestations
Coding Notes
Includes
Conditions included under this code
- mucoviscidosis
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Code Also
A second code may be required; sequencing depends on circumstances
Related Codes(3)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(89)
SNOMED CT
- PHT - Portal hypertension34742003
- Portal hypertension34742003
- Pancreatic insufficiency37992001
- Gastritis caused by Helicobacter89538001
- Helicobacter-associated gastritis89538001
- Venous hypertension234072000
- Cystic fibrosis of pancreas235978006
- Fibrocystic disease of pancreas235978006
- Fibrocystic disease of the pancreas235978006
- Mucoviscidosis of pancreas235978006
- Male infertility of genetic origin236792002
- Azoospermia with absent vasa in association with cystic fibrosis trait236793007
- Congenital obstructive azoospermia236807008
- Liver disease due to cystic fibrosis427022004
- Arthropathy associated with cystic fibrosis698940002
- Male infertility due to cystic fibrosis707418001
- Male infertility in classical cystic fibrosis707418001
- Osteoporosis due to cystic fibrosis707419009
- Osteoporosis in classical cystic fibrosis707419009
- Portal hypertension due to cystic fibrosis707420003
- Portal hypertension in classical cystic fibrosis707420003
- Pancreatic insufficiency due to cystic fibrosis of pancreas707450006
- Otorhinolaryngological manifestation co-occurrent and due to cystic fibrosis707542004
- Otorhinolaryngological manifestation of classical cystic fibrosis707542004
- Female hypofertility due to cystic fibrosis707577004
- Female hypofertility in classical cystic fibrosis707577004
- Female infertility due to cystic fibrosis707577004
- Elevated hepatic enzymes in classical cystic fibrosis707734002
- Elevated liver enzymes level due to cystic fibrosis707734002
- Liver enzymes level above reference range due to cystic fibrosis707734002
- Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis707766007
- Exocrine pancreatic manifestation of classic cystic fibrosis707766007
- Gastritis caused by H. pylori (Helicobacter pylori)708164002
- Gastritis caused by Helicobacter pylori708164002
- Helicobacter pylori-associated gastritis708164002
- Cystic fibrosis with gastritis and megaloblastic anaemia syndrome720401009
- Cystic fibrosis with gastritis and megaloblastic anemia syndrome720401009
- Lubani Al-Saleh Teebi syndrome720401009
- Polyneuropathy due to classical cystic fibrosis721197001
- Cirrhosis of liver due to classical cystic fibrosis1010616001
- Liver cirrhosis due to classical cystic fibrosis1010616001
- Female infertility due to genetic disease1148858008
- Cystic fibrosis screen positive, inconclusive diagnosis16434671000119101
- Cystic fibrosis transmembrane conductance regulator-related metabolic syndrome16434671000119101
Clinical Terms
- Cystic fibrosis with gastritis and megaloblastic anaemia syndrome
- Azoospermia with absent vasa in association with cystic fibrosis trait
- Otorhinolaryngological manifestation co-occurrent and due to cystic fibrosis
- Gastritis caused by Helicobacter
- Cystic fibrosis screen positive, inconclusive diagnosis
- Portal hypertension due to cystic fibrosis
- Liver enzymes level above reference range due to cystic fibrosis
- Lubani Al-Saleh Teebi syndrome
- Portal hypertension in classical cystic fibrosis
- Cirrhosis of liver due to classical cystic fibrosis
- Portal hypertension
- Arthropathy associated with cystic fibrosis
- Elevated liver enzymes level due to cystic fibrosis
- Female hypofertility in classical cystic fibrosis
- Otorhinolaryngological manifestation of classical cystic fibrosis
- Fibrocystic disease of pancreas
- Gastritis caused by Helicobacter pylori
- Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis
- Cystic fibrosis of pancreas
- Female infertility due to cystic fibrosis
- Helicobacter-associated gastritis
- Cystic fibrosis with gastritis and megaloblastic anemia syndrome
- Liver cirrhosis due to classical cystic fibrosis
- Venous hypertension
- Male infertility due to cystic fibrosis
- Pancreatic insufficiency due to cystic fibrosis of pancreas
- Fibrocystic disease of the pancreas
- Pancreatic insufficiency
- PHT - Portal hypertension
- Exocrine pancreatic manifestation of classic cystic fibrosis
- Osteoporosis due to cystic fibrosis
- Elevated hepatic enzymes in classical cystic fibrosis
- Female infertility due to genetic disease
- Liver disease due to cystic fibrosis
- Congenital obstructive azoospermia
- Osteoporosis in classical cystic fibrosis
- Mucoviscidosis of pancreas
- Cystic fibrosis transmembrane conductance regulator-related metabolic syndrome
- Gastritis caused by H. pylori (Helicobacter pylori)
- Female hypofertility due to cystic fibrosis
- Polyneuropathy due to classical cystic fibrosis
- Helicobacter pylori-associated gastritis
- Male infertility in classical cystic fibrosis
- Male infertility of genetic origin
Frequently Asked Questions
What is the ICD-10 code for cystic fibrosis with other manifestations?
The ICD-10-CM code for cystic fibrosis with other manifestations is E84.8. The full clinical description is "Cystic fibrosis with other manifestations". E84.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E84.8 mean?
ICD-10-CM code E84.8 represents “Cystic fibrosis with other manifestations”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E84.8 a billable code?
Yes, E84.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E84.8 in?
E84.8 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E84.8?
E84.8 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 E84.8 map to?
E84.8 maps to 24 SNOMED CT concepts: 698940002, 236793007, 1010616001, 236807008, 235978006, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E84.8?
E84.8 is linked to 1 UMLS Concept Unique Identifier: C0494350. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E84.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cystic fibrosis with other manifestations affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E84.8?
E84.8 maps to the ICD-11 code: CA25.Z (Cystic fibrosis, unspecified).
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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.