The Autoimmune Registry

Chronic inflammatory demyelinating polyradiculoneuropathy

Graphs for this disease are generated based on data from the All of Us database.
For more information on our data sources, please visit here.
For help with understanding the disease profile tabs and charts, please visit here.

Disease Profile Top Comorbidities Top Medications Patient Health Socioeconomic Factors

Names	Chronic inflammatory demyelinating polyradiculoneuropathy Chronic inflammatory demyelinating polyneuritis Chronic inflammatory demyelinating polyneuropathy Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination Chronic relapsing polyneuropathy Category: Nervous System
Prevalence	From 6,566 to 15,898 cases in the US (Rajabally 2009.). Female/Male ratio: 1.0x.
Age of Onset	Onset typically occurs at age 50.
Description	Chronic inflammatory demyelinating polyneuropathy is a rare neurological disease that inflames the nerve roots and peripheral nerves, damaging the myelin sheath. The destruction of the myelin sheath leads to loss of strength or sensation. Evidence of autoimmunity: T cells ICD-10 Code: G61.81 SNOMED Code: 128209004
Patient Groups	American Association of Neuromuscular and Electrodiagnostic Medicine (Non-profit) GBS-CIDP (Non-profit)
Bloggers
Symptoms	WeaknessUnsteady gaitWeakness in feetVision problemsReduced reflexesDouble visionWeakness in handsWeakness in hipPain
Resources	Link to Clinical Trials Link to PubMed
References	Link to Mayo Clinic Link to Cleveland Clinic Link to Healthline
	Profile by: Neha Ramjuttun Profile updated September 2024 Charts generated Oct 12, 2024 at 12:54 PM ET

Chronic inflammatory demyelinating polyradiculoneuropathy sex breakdown

Please wait while the Chronic inflammatory demyelinating polyradiculoneuropathy sex breakdown results are loaded

Chronic inflammatory demyelinating polyradiculoneuropathy age breakdown

Please wait while the Chronic inflammatory demyelinating polyradiculoneuropathy age breakdown results are loaded

Patient ethnicities

Please wait while the Patient ethnicities results are loaded

Join the registry!

Data Source: Graphs on this page represent data in electronic health records and self-reported survey results from the All of Us research database. As of July 2024, there are 451,000 sets of electronic health records and over 560,000 participants who have completed initial survey questions. This dataset, however, may not be representative of the US population. A snapshot of the data can be found here. To protect participant anonymity, results derived from fewer than 20 participants are not graphed.
The All of Us Research Program is supported by the National Institutes of Health, Office of the Director: Regional Medical Centers: 1 OT2 OD026549; 1 OT2 OD026554; 1 OT2 OD026557; 1 OT2 OD026556; 1 OT2 OD026550; 1 OT2 OD 026552; 1 OT2 OD026553; 1 OT2 OD026548; 1 OT2 OD026551; 1 OT2 OD026555; IAA #: AOD 16037; Federally Qualified Health Centers: HHSN 263201600085U; Data and Research Center: 5 U2C OD023196; Biobank: 1 U24 OD023121; The Participant Center: U24 OD023176; Participant Technology Systems Center: 1 U24 OD023163; Communications and Engagement: 3 OT2 OD023205; 3 OT2 OD023206; and Community Partners: 1 OT2 OD025277; 3 OT2 OD025315; 1 OT2 OD025337; 1 OT2 OD025276. In addition, the All of Us Research Program would not be possible without the partnership of its participants.

Chronic inflammatory demyelinating polyradiculoneuropathy top comorbidities/symptoms

Please wait while the Chronic inflammatory demyelinating polyradiculoneuropathy top comorbidities/symptoms results are loaded

Chronic inflammatory demyelinating polyradiculoneuropathy top autoimmune comorbidities

Please wait while the Chronic inflammatory demyelinating polyradiculoneuropathy top autoimmune comorbidities results are loaded

Join the registry!

* Disease is suspected as autoimmune, but unconfirmed.
Data Source: Graphs on this page represent data in electronic health records from the All of Us research database. As of July 2024, there are 451,000 sets of electronic health records collected from participants. In the United States, because electronic health records use billing codes for diagnoses, some conditions may not be perfectly captured by these data, especially if the condition is rare. A snapshot of the data can be found here. To protect participant anonymity, results derived from fewer than 20 participants are not graphed.
The All of Us Research Program is supported by the National Institutes of Health, Office of the Director: Regional Medical Centers: 1 OT2 OD026549; 1 OT2 OD026554; 1 OT2 OD026557; 1 OT2 OD026556; 1 OT2 OD026550; 1 OT2 OD 026552; 1 OT2 OD026553; 1 OT2 OD026548; 1 OT2 OD026551; 1 OT2 OD026555; IAA #: AOD 16037; Federally Qualified Health Centers: HHSN 263201600085U; Data and Research Center: 5 U2C OD023196; Biobank: 1 U24 OD023121; The Participant Center: U24 OD023176; Participant Technology Systems Center: 1 U24 OD023163; Communications and Engagement: 3 OT2 OD023205; 3 OT2 OD023206; and Community Partners: 1 OT2 OD025277; 3 OT2 OD025315; 1 OT2 OD025337; 1 OT2 OD025276. In addition, the All of Us Research Program would not be possible without the partnership of its participants.
Anti-inflammatory / specialty medications and supplements

Please wait while the Anti-inflammatory / specialty medications and supplements results are loaded

Chronic inflammatory demyelinating polyradiculoneuropathy top immunosuppressants / autoimmune therapies

Please wait while the Chronic inflammatory demyelinating polyradiculoneuropathy top immunosuppressants / autoimmune therapies results are loaded

Join the registry!

* Biologic medications.
Data Source: Graphs on this page represent data in electronic health records from the All of Us research database. As of July 2024, there are 451,000 sets of electronic health records collected from participants. A snapshot of the data can be found here. To protect participant anonymity, results derived from fewer than 20 participants are not graphed.
The All of Us Research Program is supported by the National Institutes of Health, Office of the Director: Regional Medical Centers: 1 OT2 OD026549; 1 OT2 OD026554; 1 OT2 OD026557; 1 OT2 OD026556; 1 OT2 OD026550; 1 OT2 OD 026552; 1 OT2 OD026553; 1 OT2 OD026548; 1 OT2 OD026551; 1 OT2 OD026555; IAA #: AOD 16037; Federally Qualified Health Centers: HHSN 263201600085U; Data and Research Center: 5 U2C OD023196; Biobank: 1 U24 OD023121; The Participant Center: U24 OD023176; Participant Technology Systems Center: 1 U24 OD023163; Communications and Engagement: 3 OT2 OD023205; 3 OT2 OD023206; and Community Partners: 1 OT2 OD025277; 3 OT2 OD025315; 1 OT2 OD025337; 1 OT2 OD025276. In addition, the All of Us Research Program would not be possible without the partnership of its participants.
Quick links: Patient-reported 7-day average pain Patient-reported 7-day average fatigue General physical health General mental health Social and relationship satisfaction General quality of life Ability to carry out social roles and activities

Quick Links
Patient-reported 7-day average pain Patient-reported 7-day average fatigue General physical health General mental health Social and relationship satisfaction General quality of life Ability to carry out social roles and activities

Patient-reported 7-day average pain

Please wait while the Patient-reported 7-day average pain results are loaded

Patient-reported 7-day average fatigue

Please wait while the Patient-reported 7-day average fatigue results are loaded

General physical health

Please wait while the General physical health results are loaded

General mental health

Please wait while the General mental health results are loaded

Social and relationship satisfaction

Please wait while the Social and relationship satisfaction results are loaded

General quality of life

Please wait while the General quality of life results are loaded

Ability to carry out social roles and activities

Please wait while the Ability to carry out social roles and activities results are loaded

Join the registry!

Data Source: Graphs on this page represent data in self-reported survey results from the All of Us research database. As of July 2024, there are 560,000 participants who have completed these surveys. This dataset, however, may not be representative of the US population. A snapshot of the data can be found here. To protect participant anonymity, results derived from fewer than 20 participants are not graphed.
The All of Us Research Program is supported by the National Institutes of Health, Office of the Director: Regional Medical Centers: 1 OT2 OD026549; 1 OT2 OD026554; 1 OT2 OD026557; 1 OT2 OD026556; 1 OT2 OD026550; 1 OT2 OD 026552; 1 OT2 OD026553; 1 OT2 OD026548; 1 OT2 OD026551; 1 OT2 OD026555; IAA #: AOD 16037; Federally Qualified Health Centers: HHSN 263201600085U; Data and Research Center: 5 U2C OD023196; Biobank: 1 U24 OD023121; The Participant Center: U24 OD023176; Participant Technology Systems Center: 1 U24 OD023163; Communications and Engagement: 3 OT2 OD023205; 3 OT2 OD023206; and Community Partners: 1 OT2 OD025277; 3 OT2 OD025315; 1 OT2 OD025337; 1 OT2 OD025276. In addition, the All of Us Research Program would not be possible without the partnership of its participants.
Quick links: Concerns about ability to pay Feeling unheard by healthcare providers Patient employment status Patient insurance coverage

Quick Links
Concerns about ability to pay Feeling unheard by healthcare providers Patient employment status Patient insurance coverage

Concerns about ability to pay

Please wait while the Concerns about ability to pay results are loaded

Feeling unheard by healthcare providers

Please wait while the Feeling unheard by healthcare providers results are loaded

Patient employment status

Please wait while the Patient employment status results are loaded

Patient insurance coverage

Please wait while the Patient insurance coverage results are loaded

Join the registry!

Data Source: Graphs on this page represent data in electronic health records and self-reported survey results from the All of Us research database. As of July 2024, there are 451,000 sets of electronic health records and over 560,000 participants who have completed initial survey questions. This dataset, however, may not be representative of the US population. A snapshot of the data can be found here. To protect participant anonymity, results derived from fewer than 20 participants are not graphed.
The All of Us Research Program is supported by the National Institutes of Health, Office of the Director: Regional Medical Centers: 1 OT2 OD026549; 1 OT2 OD026554; 1 OT2 OD026557; 1 OT2 OD026556; 1 OT2 OD026550; 1 OT2 OD 026552; 1 OT2 OD026553; 1 OT2 OD026548; 1 OT2 OD026551; 1 OT2 OD026555; IAA #: AOD 16037; Federally Qualified Health Centers: HHSN 263201600085U; Data and Research Center: 5 U2C OD023196; Biobank: 1 U24 OD023121; The Participant Center: U24 OD023176; Participant Technology Systems Center: 1 U24 OD023163; Communications and Engagement: 3 OT2 OD023205; 3 OT2 OD023206; and Community Partners: 1 OT2 OD025277; 3 OT2 OD025315; 1 OT2 OD025337; 1 OT2 OD025276. In addition, the All of Us Research Program would not be possible without the partnership of its participants.