Skip to main content
U.S. Department of Health & Human Services
National Institutes of Health
NCATS

COVID-19 is an emerging, rapidly evolving situation.

Get the latest public health information from CDC: https://www.coronavirus.gov (link is external)
Get the latest research information from NIH: https://www.nih.gov/coronavirus (link is external)

National Center for Advancing and Translational Sciences National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences
1-888-205-2311
Menu Search
1-888-205-2311
Menu
  • Home
  • Diseases expand submenu for Diseases
    • Browse A-Z
    • Find Diseases By Category expand submenu for Find Diseases By Category
      • Autoimmune / Autoinflammatory diseases
      • Bacterial infections
      • Behavioral and mental disorders
      • Blood Diseases
      • Chromosome Disorders
      • Congenital and Genetic Diseases
      • Connective tissue diseases
      • Digestive Diseases
      • Ear, Nose, and Throat Diseases
      • Endocrine Diseases
      • Environmental Diseases
      • Eye diseases
      • Female Reproductive Diseases
      • Fungal infections
      • Heart Diseases
      • Hereditary Cancer Syndromes
      • Immune System Diseases
      • Kidney and Urinary Diseases
      • Lung Diseases
      • Male Reproductive Diseases
      • Metabolic disorders
      • Mouth Diseases
      • Musculoskeletal Diseases
      • Myelodysplastic Syndromes
      • Nervous System Diseases
      • Newborn Screening
      • Nutritional diseases
      • Parasitic diseases
      • Rare Cancers
      • RDCRN
      • Skin Diseases
      • Viral infections
    • List of FDA Orphan Drugs
    • GARD Information Navigator
    • FAQs About Rare Diseases
  • Guides expand submenu for Guides
    • Patients, Families and Friends expand submenu for Patients, Families and Friends
      • How to Find a Disease Specialist
      • Tips for the Undiagnosed
      • Support for Patients and Families
      • Tips for Finding Financial Aid
      • Help with Travel Costs
      • How to Get Involved in Research
      • FAQs About Chromosome Disorders
      • Medical and Science Glossaries
    • Healthcare Professionals expand submenu for Healthcare Professionals
      • Caring for Your Patient with a Rare Disease
      • ICD Coding for Rare Diseases
      • FindZebra Diagnosis Assist Tool
    • Researchers expand submenu for Researchers
      • Finding Funding Opportunities
    • Teachers and Students expand submenu for Teachers and Students
      • Teaching Resources
  • News expand submenu for News
    • In The Spotlight
    • News Archive
    • Connect with GARD
    • Media Requests
  • About GARD expand submenu for About GARD
    • Contact GARD
    • About GARD
    • Videos
    • Brochures and Publications
  • En Español expand submenu for En Español
    • Enfermedades
    • Contacte GARD
    • Guías de Información expand submenu for Guías de Información
      • Preguntas Más Frecuentes Sobre Enfermedades Raras
      • Como Encontrar un Especialista en su Enfermedad
      • Consejos Para una Condición no Diagnosticada
      • Consejos Para Pacientes y Familias
      • Consejos Para Obtener Ayuda Financiera Para Una Enfermedad
      • Participe en Estudios de Investigación
      • Preguntas Más Frecuentes Sobre los Trastornos Cromosómicos
    • Sobre GARD
  • Home
© Positive Exposure
banner showing people with disabilities and/or their relatives
  1. Home
  2. Guides
  3. Healthcare Professionals
  4. ICD Coding for Rare Diseases
print
  • Patients, Families and Friends expand submenu for Patients, Families and Friends
    • How to Find a Disease Specialist
    • Tips for the Undiagnosed
    • Support for Patients and Families
    • Tips for Finding Financial Aid
    • Help with Travel Costs
    • How to Get Involved in Research
    • FAQs About Chromosome Disorders
    • Medical and Science Glossaries
  • Healthcare Professionals expand submenu for Healthcare Professionals
    • Caring for Your Patient with a Rare Disease
    • ICD Coding for Rare Diseases
    • FindZebra Diagnosis Assist Tool
  • Researchers expand submenu for Researchers
    • Finding Funding Opportunities
  • Teachers and Students expand submenu for Teachers and Students
    • Teaching Resources

ICD Coding for Rare Diseases


Listen

ICD Coding for Rare Diseases

You need to have an ICD code for your patient’s medical records—it is important for health insurance reimbursement, administration, epidemiology, and research. Finding the best ICD code for a patient who has a rare disease can often be a challenge. Many rare diseases are not included in the World Health Organization’s (WHO’s) International Classification of Diseases (ICD). Of the approximately 7,000 rare diseases, only about 500 have a specific code.[1] 

Different versions of the ICD code exist worldwide. The United States currently uses the ICD-10-CM, a Clinical Modification of the WHO standard for diagnoses adapted for insurance reimbursement and billing purposes. This version allows for further breakdown of a code, which increases diagnosis specificity. You may find published material that references ICD-9-CM codes, which were used before October 1, 2015; however, not every code in the ICD-9-CM has a corresponding code in ICD-10-CM. Europe and other parts of the world use the ICD-10. The root codes for ICD-10 and ICD-10-CM are the same, making it helpful for locating codes for general body systems and disease processes. 


What should I do if a rare disease does not have an ICD code?
A good place to start is to contact an advocacy organization for the rare disease. These organizations are often aware of how the condition has been coded for other patients with the same diagnosis and may be able to recommend one or more codes to use. Many disease advocacy organizations also have medical advisory boards or physician directories, which may be able to direct you to someone with experience coding for that particular condition. You can search the GARD website for a list of disease advocacy organizations. If you don’t find a specific group, contact a GARD Information Specialist.

See our page on How to Find a Disease Specialist for more tips on how to find a healthcare professional who sees patients with a particular rare condition. 

Orphanet is a European reference portal for information on rare diseases and orphan drugs. Orphanet outlines the ICD-10 coding rules for rare diseases included in their database. The Orphanet database also often includes coding information for the Online Mendelian Inheritance in Man (OMIM), the Unified Medical Language System (UMLS), and more.

When a diagnosis has not been established, or when a code does not exist for a specific rare disease, general coding guidelines indicate that it is acceptable to use codes that describe signs and symptoms. You may want to review this article from the American Academy of Professional Coders (AAPC) titled ICD-10-CM Coding Tips: Signs and Symptoms. As a general rule, code up to the highest number of digits you can and list only the most common signs and symptoms.



When will more ICD codes for rare diseases be released? 
ICD-11 is scheduled to be released in 2018. It is expected to have a tenfold increase in the number of rare diseases that are currently in ICD-10. So far, 5,400 rare diseases from the Orphanet database are present in the foundation layer of ICD-11.[2]  The WHO established a Topic Advisory Group for Rare Diseases composed of international experts, who will add more rare diseases over time.  


Where can I find an ICD code? 
Several online resources can help you find ICD codes:

  • WHO ICD-10 Version: 2016 – A searchable online version of ICD-10 that allows users to search by hierarchy or by entering the disease name.
  • List of Official ICD-10 Updates - ICD-10 updates endorsed by the WHO.
  • ICD10Data.com – A website created to make it easier to quickly find medical coding information. The website is also smartphone- and tablet-friendly.
  • Orphanet – A European reference portal for information on rare diseases and orphan drugs that includes ICD-10 codes, disease summaries, prevalence data, and more. Some of the ICD-10 codes given to a disease are assigned by Orphanet and not the WHO.


  • References:

    1. Bearryman E. Does your rare disease have a code? EURORDIS. March 2, 2015. http://www.eurordis.org/news/does-your-rare-disease-have-code 

    2. Aymé S, Bellet B, and Rath A. Rare diseases in ICD11: making rare diseases visible in health information systems through appropriate coding. Orphanet Journal of Rare Diseases. 2015. 10:35 http://ojrd.biomedcentral.com/articles/10.1186/s13023-015-0251-8 Last updated: 6/24/2016

    Share this content:

    Share this content:

    twitter-icon facebook-icon contact-icon link-icons

    Copy Link

    Link copied to your clipboard.

    printer-icon

    You May Be Interested In

    How to Find a Disease Specialist

    How to Find a Disease Specialist

    Tips for the Undiagnosed

    Tips for the Undiagnosed

    Support for Patients and Families

    Support for Patients and Families

    Tips for Finding Financial Aid

    Tips for Finding Financial Aid

    Help with Travel Costs

    Help with Travel Costs

    How to Get Involved in Research

    How to Get Involved in Research

    FAQs About Chromosome Disorders

    FAQs About Chromosome Disorders

    Medical and Science Glossaries

    Medical and Science Glossaries

    Caring for Your Patient with a Rare Disease

    Caring for Your Patient with a Rare Disease

    ICD Coding for Rare Diseases

    ICD Coding for Rare Diseases

    FindZebra Diagnosis Assist Tool

    FindZebra Diagnosis Assist Tool

    Finding Funding Opportunities

    Finding Funding Opportunities

    Teaching Resources

    Teaching Resources

    placeholder for the horizontal scroll slider Back to top
    GARD Home NCATS Home Site Map Browse Glossary A-Z Privacy Notice Disclaimer Accessibility FOIA OIG

    If you have problems viewing PDF files, download the latest version of Adobe Reader

    For language access assistance, contact the NCATS Public Information Officer

    Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311

    contact gard Office of Rare Disease Research Facebook Page Office of Rare Disease Research on Twitter
    Listen