ORPHA:36258
Buerger disease
Also known as: Thromboangiitis obliterans
Publications
5,600
93.5th percentile
Trials
11
Interventional, condition-specific
Researchers
952
Distinct authors in sample
Gene link
—
Readiness
2/6
Stages with a signal
Clinical definition (Orphanet)
A rare systemic disease characterized by inflammatory, non-necrotizing, non-atherosclerotic, occlusive vascular disease with thrombosis and recanalization affecting small and medium sized arteries and veins of upper and lower extremities.
How rare: 1-5 / 10 000 — about one to five people per ten thousand (still uncommon, but less ultra-rare).
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0008889
- MeSH:D013919
- OMIM:211480
- UMLS:C0040021
- NCIT:C35070
Additional Mondo synonyms (4)
Buerger's Disease · Buerger's disease · thromboangiitis obliterans · thromboangiitis obliterans [Buerger's disease]
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.”
2/6 stages with a signal
An interventional trial matched this condition name on ClinicalTrials.gov — see trials below.
- Gene identifiedNot found
No GenCC disease–gene assertion in this build
- LiteraturePresent
5,600 matched papers (1,149 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialPresent
11 matched on ClinicalTrials.gov (3 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)
Not enriched in this build — Monarch phenotype joins were not run for this record.
Animal models (Monarch / Alliance)
Not enriched in this build.
Literature
Is anyone studying this?
5,600
5,600 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=5449) is 41.
5,600 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).
1,149 in the last 10 years · medium confidence · 93.5th percentile (publications denominator)
Phrase hits: 5,600 · MeSH hits: 0
Who's working on it?
952
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.
- 01Li J6 papers · 2026
Department of General Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai Key Laboratory of Vascular Lesions Regulation and Remodeling, Shanghai, 201399, China.
Papers in Europe PMC - 02Zhang Y6 papers · 2026
Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Papers in Europe PMC - 03Chen J5 papers · 2026
Guangzhou Institute of Cardiovascular Disease, Guangdong Key Laboratory of Vascular Diseases, State Key Laboratory of Respiratory Disease, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China. Electronic address: 2021390029@gzhmu.edu.cn.
Papers in Europe PMC - 04Ghaderi A5 papers · 2026
Department of Addiction Studies, School of Medical, Kashan University of Medical Sciences, Kashan, Iran.
Papers in Europe PMC - 05Ghorbani S5 papers · 2026
Biostatistics, Cancer Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Papers in Europe PMC - 06Liu Z5 papers · 2026
Guangdong Provincial Key Laboratory of Translational Cancer Research of Chinese Medicines, Joint International Research Laboratory of Translational Cancer Research of Chinese Medicines, International Institute for Translational Chinese Medicine, School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China. Electronic address: liuzq@gzucm.edu.cn.
Papers in Europe PMC - 07Wei Z5 papers · 2026
Department of Burns and Plastic Surgery, The Affiliated Hospital of Zunyi Medical College, Zunyi, China.
Papers in Europe PMC - 08Asadollahi Shahir AA4 papers · 2026
Department of Addiction Studies, School of Medical, Kashan University of Medical Sciences, Kashan, Iran.
Papers in Europe PMC - 09Chen B4 papers · 2026
Department of General Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai Key Laboratory of Vascular Lesions Regulation and Remodeling, Shanghai, 201399, China.
Papers in Europe PMC - 10Liu X4 papers · 2026
Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Papers in Europe PMC
Clinical research
Is a treatment being tested?
11
interventional trials for this specific condition
11 interventional trials matched this specific condition name; 3 currently recruiting in our sample.
Data as of 27 July 2026
11 interventional trials — more than 73% of diseases in the trials denominator have none at all (5114 of 7003; this disease is at the 92.1th percentile).
medium confidence · 92.1th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
11 interventional trials matched after quoted-phrase search and title/condition post-filter.
- NCT05854615·RECRUITING·Efficacy and Safety of Stempeucel® in Patients With Critical Limb Ischemia (CLI) Due to Buerger's Disease
Conditions: Critical Limb Ischemia · Buerger's Disease·Matched via name phrase
- NCT05698979·NOT YET RECRUITING·Evaluation of Botulinum TOXin Type A in the Treatment of Buerger's Disease
Conditions: Buerger Disease · Raynaud Syndrome·Matched via name phrase
- NCT07215923·RECRUITING·A First in Human Single Ascending Dose (SAD) Study of ATI-1013 in Healthy Smokers
Conditions: Thromboangiitis Obliterans (Buerger's Disease)·Matched via name phrase
Observational and natural-history studies
4 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
- NCT07023965·ENROLLING BY INVITATION·Follow-up Study Using Gene Therapy for Critical Limb Ischemia (NL003-CLI-III-L)
Conditions: Peripheral Arterial Disease(PAD) · Arterial Occlusive Disease · Arteriosclerosis Obliterans · Thromboangiitis Obliterans·Matched via name phrase
Where to find support
We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:
India — NPRD
Last verified 2026-07-26This 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.
"Buerger disease" OR "Thromboangiitis obliterans" OR "Buerger's Disease" OR "thromboangiitis obliterans [Buerger's disease]"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Buerger disease" OR "Thromboangiitis obliterans" OR "Buerger's Disease" OR "thromboangiitis obliterans [Buerger's disease]"
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: 11 interventional · 4 observational · 1 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
Ingested 2026-07-26T23:52:25.210Z
