RARE DISEASERESEARCH ATLAS

ORPHA:3299

Tetanus

low confidenceDisorder

Publications

94,099

Trials

247

Interventional, condition-specific

Researchers

1,482

Distinct authors in sample

Gene link

Readiness

3/6

Stages with a signal

Clinical definition (Orphanet)

A toxin-mediated infection due to the anaerobic bacteria Clostridium tetani and characterized by spasms and contractions of the skeletal muscles, the disease is often lethal.

How rare: <1 / 1 000 000 — fewer than one in a million. In a city the size of Kolkata, that might mean on the order of fifteen people.

Orphanet entry

Cross-references

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

Additional Mondo synonyms (2)

Clostridium tetani caused infectious disease of the nervous system · Clostridium tetani infectious disease of the nervous system

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

    94,099 matched papers (31,681 in last 10 years) Source

  3. Phenotype characterisedPresent

    30 HPO annotations (e.g. Dysphagia; Humoral immunodeficiency; Intermittent painful muscle spasms) 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

    247 matched on ClinicalTrials.gov (22 recruiting in sample)

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)

30

Associated phenotypes · MONDO:0005526

  • Dysphagia
  • Humoral immunodeficiency
  • Intermittent painful muscle spasms
  • Autonomic bladder dysfunction
  • Laryngospasm

Showing 5 of 30 — 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

8

Drugs / clinical candidates · MONDO_0005526

CTD chemicals (MyDisease.info)

10 associated chemicals. Therapeutic evidence is listed first when present — not a treatment recommendation.

  • Baclofen · therapeutic
  • Barbiturates · therapeutic
  • Diazepam · therapeutic
  • Labetalol · therapeutic
  • Magnesium Sulfate · therapeutic
  • Midazolam · therapeutic
  • Pancuronium · therapeutic
  • Propofol · therapeutic
  • Vecuronium Bromide · therapeutic
  • Tetanus Toxin · marker/mechanism

MyDisease.info · MONDO:0005526

Literature

Is anyone studying this?

94,099

94,099 papers — among the better-studied rare conditions, though still a fraction of common-disease literature (breast cancer: over 700,000). Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=3967) is 59.

94,099 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).

31,681 in the last 10 years · low confidence

Phrase hits: 94,099 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

1,482

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
    Li Y7 papers · 2026

    Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, China.

    Papers in Europe PMC
  2. 02
    Wang Y7 papers · 2026

    Henan Province Center for Disease Control and Prevention, Zhengzhou, People's Republic of China.

    Papers in Europe PMC
  3. 03
    Zhang Y7 papers · 2026

    China National Biotec Group Company Limited, Beijing, China.

    Papers in Europe PMC
  4. 04
    Zhu Y7 papers · 2026

    Optum Life Sciences, Eden Prairie, MN, USA.

    Papers in Europe PMC
  5. 05
    Wang X6 papers · 2026

    Wuhan Institute of Biological Products Co., Ltd, Hubei, China.

    Papers in Europe PMC
  6. 06
    Chen Y5 papers · 2026

    Emergency Department, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

    Papers in Europe PMC
  7. 07
    Huang Y5 papers · 2026

    Beijing Institute for Brain Research, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

    Papers in Europe PMC
  8. 08
    Li H5 papers · 2026

    Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin, 300384, PR China.

    Papers in Europe PMC
  9. 09
    Li J5 papers · 2026

    The Second Clinical Medical School of Shandong University, Jinan, China.

    Papers in Europe PMC
  10. 10
    Liu C5 papers · 2026

    Department of Emergency, Peking University First Hospital, Beijing, 100034, PR China. Electronic address: Chengliu218@pku.edu.cn.

    Papers in Europe PMC

Clinical research

Is a treatment being tested?

247

interventional trials for this specific condition

247 interventional trials matched this specific condition name; 22 currently recruiting in our sample.

Data as of 11 September 2026

247 interventional trials — more than 77.2% of diseases in the trials denominator have none at all (5501 of 7126; this disease is at the 99.5th percentile).

low confidence · 99.5th percentile (trials denominator)

Recruiting interventional trials

From the matched ClinicalTrials.gov set

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

Observational and natural-history studies

26 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 64 · after dedupe 64 · already on CT.gov 0 · kept 0 · parent 0 · uncertain 64 · dropped 0 · fetched 2026-07-29

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 (64)

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 Tetanus — 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.

"Tetanus" OR "Clostridium tetani caused infectious disease of the nervous system" OR "Clostridium tetani caused infectious disease of nervous system" OR "Clostridium tetani infectious disease of the nervous system" OR "Clostridium tetani infectious disease of nervous system"

Run this search on Europe PMC

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

"Tetanus" OR "Clostridium tetani caused infectious disease of the nervous system" OR "Clostridium tetani caused infectious disease of nervous system" OR "Clostridium tetani infectious disease of the nervous system" OR "Clostridium tetani infectious disease of nervous system"

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: 247 interventional · 26 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

Confidence reasoning

  • Preferred label is short or not clearly distinctive
  • No synonyms dropped by stoplist
  • No label/synonym collisions with other diseases in this corpus
  • Publication count (94099) is implausibly high for prevalence class "<1 / 1 000 000" — treat as possible over-matching, not a measure of research intensity

Ingested 2026-07-26T22:47:04.185Z