E84.19

Billable

Cystic fibrosis with other intestinal manifestations

Cystic fibrosis with other intestinal manifestations

Status

Billable / Specific

Block

E70-E88

Parent Code

E84.1

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Distal intestinal obstruction syndrome

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

Code Also

A second code may be required; sequencing depends on circumstances

Related Codes(1)
E84.11

Meconium ileus in cystic fibrosis

Billable
Also Known As / Clinical Terms(27)

SNOMED CT

UMLS

Clinical Terms

  • DIOS (distal intestinal obstruction syndrome) due to cystic fibrosis
  • Digestive system manifestation co-occurrent and due to cystic fibrosis
  • MIE - Meconium ileus equivalent
  • Digestive manifestation of classical cystic fibrosis
  • Meconium ileus equivalent syndrome
  • Distal intestinal obstruction syndrome due to cystic fibrosis
  • Distal intestinal obstruction syndrome
  • Fibrosing colonopathy
  • DIOS - Distal intestinal obstruction syndrome
  • Distal intestinal obstruction syndrome (disorder)
  • Meconium ileus equivalent
Frequently Asked Questions
What is the ICD-10 code for cystic fibrosis with other intestinal manifestations?

The ICD-10-CM code for cystic fibrosis with other intestinal manifestations is E84.19. The full clinical description is "Cystic fibrosis with other intestinal manifestations". E84.19 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E84.19 mean?

ICD-10-CM code E84.19 represents “Cystic fibrosis with other intestinal 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 E84.19 a billable code?

Yes, E84.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E84.19 in?

E84.19 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E84.19?

E84.19 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 E84.19 map to?

E84.19 maps to 4 SNOMED CT concepts: 817966005, 233662009, 707536003, 445090007. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E84.19?

E84.19 is linked to 2 UMLS Concept Unique Identifiers: C2874308, C0398349. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E84.19 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cystic fibrosis with other intestinal 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 E84.19?

There is no direct ICD-11 mapping available for E84.19 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.