RARE DISEASERESEARCH ATLAS

ORPHA:98916

Acute inflammatory demyelinating polyradiculoneuropathy

medium confidenceDisorder

Also known as: AIDP · Acute idiopathic demyelinating polyneuropathy · Acute inflammatory polyneuropathy · GBS, acute inflammatory demyelinating polyradiculoneuropathic form · Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form

Publications

4,615

92.3th percentile

Trials

1

Interventional, condition-specific

Researchers

986

Distinct authors in sample

Gene link

Readiness

3/6

Stages with a signal

Clinical definition (Orphanet)

A rare inflammatory belonging to the clinical spectrum of Guillain-Barré syndrome (GBS).

How rare: 1-9 / 100 000 — about one to nine people per hundred thousand.

Orphanet entry

Cross-references

Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.

Additional Mondo synonyms (4)

Guillain-Barre syndrome, acute inflammatory demyelinating polyradiculoneuropathic form · acute idiopathic demyelinating polyneuropathy · acute inflammatory demyelinating polyradiculopathy · acute inflammatory polyneuropathy

Research stages

Trial readiness signals

Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”

3/6 stages with a signal

An interventional trial matched this condition name on ClinicalTrials.gov — see trials below.

  1. Gene identifiedNot found

    No GenCC disease–gene assertion in this build

  2. LiteraturePresent

    4,615 matched papers (3,020 in last 10 years) Source

  3. Phenotype characterisedPresent

    13 HPO annotations (e.g. Distal lower limb muscle weakness; Dysesthesia; Impaired oropharyngeal swallow response) Source

  4. Animal modelNot found

    No Alliance genotype “model of” associations via Monarch for these Mondo IDs

  5. Orphan designationNot found

    No FDA or EMA orphan-drug designation matched this disease via UMLS or preferred name Source

  6. Interventional trialPresent

    1 matched on ClinicalTrials.gov

Biology

Genes and phenotypes

Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.

Do we know what causes it?

Not yet — the cause hasn't been pinned down in GenCC.

No strong gene–disease assertion joined for this Orphanet entity.

Phenotypes (Monarch / HPO)

13

Associated phenotypes · MONDO:0020347

  • Distal lower limb muscle weakness
  • Dysesthesia
  • Impaired oropharyngeal swallow response
  • Onion bulb formation
  • Gait ataxia

Showing 5 of 13 — open Monarch for the full list.

Animal models (Monarch / Alliance)

None returned for this Mondo ID. Empty here is not proof that no model organism work exists under another name or gene.

Monarch fetch 2026-07-29

Therapies

Designations, candidates, and chemicals

FDA OOPD and EMA orphan designations, Open Targets clinical candidates, and CTD chemical associations via MyDisease.info. These never change the interventional-trial headline.

Orphan designation (FDA · EMA)

No designation matched this disease via UMLS or preferred name on the FDA OOPD mirror or EMA orphan register. Absence here is not proof that none exists under another wording.

Open Targets candidates

No drugs or clinical candidates returned for this Mondo ID on Open Targets.

CTD chemicals (MyDisease.info)

No CTD chemical associations returned for this Mondo ID.

Literature

Is anyone studying this?

4,615

4,615 papers have been published on this condition. That is a real research literature — still far smaller than common diseases (breast cancer: over 700,000 papers). Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=3967) is 59.

4,615 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 59 (publications denominator n=3967).

3,020 in the last 10 years · medium confidence · 92.3th percentile (publications denominator)

Phrase hits: 4,615 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

986

Distinct author names in 200 sampled papers — named people below.

Who's working on it?

People publishing on this condition (sampled Europe PMC records). Affiliation is the most recent found in that sample.

  1. 01
    Wang Y10 papers · 2026

    Department of Orthopedic Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin Medical University, Harbin, 150000, P. R. China.

    Papers in Europe PMC
  2. 02
    Liu Y4 papers · 2026

    Department of Orthopedic Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin Medical University, Harbin, 150000, P. R. China.

    Papers in Europe PMC
  3. 03
    Yang X4 papers · 2026

    Department of Otolaryngology, Beijing Anzhen Nanchong Hospital, Capital Medical University and Nanchong Central Hospital, The Affiliated Nanchong Central Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.

    Papers in Europe PMC
  4. 04
    Zhou Y4 papers · 2025

    Department of Neurology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

    Papers in Europe PMC
  5. 05
    Chen X3 papers · 2025

    Department of Geriatric Medicine, Rotherham General Hospital, Moorgate Road, Rotherham S60 2UD, UK.

    Papers in Europe PMC
  6. 06
    Kalita J3 papers · 2024

    Department of Neurology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.

    Papers in Europe PMC
  7. 07
    Kumar M3 papers · 2023

    Department of Neurology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.

    Papers in Europe PMC
  8. 08
    Misra UK3 papers · 2024

    Department of Neurology, Apollomedics Super Specialty Hospitals, Lucknow, India.

    Papers in Europe PMC
  9. 09
    Yang J3 papers · 2026

    Department of Rheumatology and Immunology, The Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.

    Papers in Europe PMC
  10. 10
    Zhang J3 papers · 2026

    Department of Occupational and Environmental Health and Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, School of Public Health, Fourth Military Medical University, Xi'an, 710032, China. zjbin777@fmmu.edu.cn.

    Papers in Europe PMC

Clinical research

Is a treatment being tested?

1

interventional trials for this specific condition

1 interventional trial matched this specific condition name; none in our sample are currently recruiting.

Data as of 11 September 2026

1 interventional trial — more than 77.2% of diseases in the trials denominator have none at all (5501 of 7126; this disease is at the 80.1th percentile).

medium confidence · 80.1th percentile (trials denominator)

Recruiting interventional trials

From the matched ClinicalTrials.gov set

1 interventional trials matched after quoted-phrase search and title/condition post-filter.

No currently recruiting studies in the matched set. Open the same search on ClinicalTrials.gov.

Observational and natural-history studies

2 observational studies match this condition. These do not test a treatment and are not counted in the interventional-trial headline, but they are genuine research: natural-history work often defines the endpoints needed for a future rare-disease trial, and families may be able to enroll.

Recruiting or not-yet-recruiting

Open the complete matched search on ClinicalTrials.gov

Other registries (secondary)

Broader net from EU CTIS, ISRCTN, and ICTRP when available — deduped against ClinicalTrials.gov IDs already counted above. Dual-model LLM relevance gates what we keep. These rows are not added to the interventional headline.

raw 5 · after dedupe 5 · already on CT.gov 0 · kept 0 · parent 0 · uncertain 5 · dropped 0 · fetched 2026-07-30

Source notes: ictrp: Error: ICTRP public search unavailable (WHO portal is SPA-only; SOAP needs partnership). Tried: https://apps.who.int/tri

No secondary-registry studies passed dual-model relevance for this condition name (after dedupe).

Uncertain / not reviewed (5)

Where to find support

Condition-specific patient organisations, when Orphanet lists them, are on the disease’s Orphanet page. We also link umbrella groups that support undiagnosed and ultra-rare families.

Orphanet entry for Acute inflammatory demyelinating polyradiculoneuropathy — check Associations / patient organisations on that page.

India — NPRD

Last verified 2026-07-26

This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.

Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.

How we counted this

Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.

"Acute inflammatory demyelinating polyradiculoneuropathy" OR "Acute idiopathic demyelinating polyneuropathy" OR "Acute inflammatory polyneuropathy" OR "GBS, acute inflammatory demyelinating polyradiculoneuropathic form" OR "Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form" OR "Guillain-Barre syndrome, acute inflammatory demyelinating polyradiculoneuropathic form" OR "acute inflammatory demyelinating polyradiculopathy"

Run this search on Europe PMC

ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):

"Acute inflammatory demyelinating polyradiculoneuropathy" OR "Acute idiopathic demyelinating polyneuropathy" OR "Acute inflammatory polyneuropathy" OR "GBS, acute inflammatory demyelinating polyradiculoneuropathic form" OR "Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form" OR "Guillain-Barre syndrome, acute inflammatory demyelinating polyradiculoneuropathic form" OR "acute inflammatory demyelinating polyradiculopathy"

Interventional trials matched via: phrase (mesh = registered under a MeSH descriptor no name phrase would catch; recall-expansion = gene / selected parent terms used only for trials).

Study-type breakdown: 1 interventional · 2 observational · 0 expanded access. Only interventional studies enter the trial headline.

Query health: ok — strategies attempted: phrase; with hits: phrase

Run this search on ClinicalTrials.gov

Synonyms dropped by stoplist: AIDP

Confidence reasoning

  • Preferred label is multi-word and distinctive
  • 1 synonym(s) dropped by stoplist (may under-count)
  • No label/synonym collisions with other diseases in this corpus

Ingested 2026-07-27T05:43:24.802Z