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K90.0

Billable

Celiac disease

HCC Category Mapping

RxHCCHCC 66Pancreatic Disease and Disorders
0.000

What This Code Means

An autoimmune condition where the small intestine cannot properly digest gluten (a protein in wheat, barley, and rye), causing malabsorption and digestive symptoms.

Coding Tips

  • Document whether the patient is on a gluten-free diet and compliance status
  • Link to associated conditions such as dermatitis herpetiformis (L13.0) or nutritional deficiencies when present

Clinical Significance

Celiac disease is an autoimmune condition where gluten triggers small intestine inflammation, leading to malabsorption and nutritional deficiencies. This lifelong condition requires strict gluten-free diet adherence and monitoring for complications including lymphoma and osteoporosis.

Documentation Requirements

  • Positive celiac serology (anti-tissue transglutaminase, anti-endomysial antibodies)
  • Small bowel biopsy showing villous atrophy
  • Clinical response to gluten-free diet
  • Symptoms of malabsorption (diarrhea, weight loss, bloating)
  • Evidence of nutritional deficiencies (iron, B12, folate, vitamin D)
  • Genetic testing (HLA-DQ2/DQ8) when performed
  • Exclusion of other causes of malabsorption
  • Documentation of gluten exposure history

Use Additional Code

  • code for associated disorders including:
  • dermatitis herpetiformis (L13.0)
  • gluten ataxia (G32.81)

Code Also

  • exocrine pancreatic insufficiency (K86.81)

Commonly Confused Codes

Code Hierarchy

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