ORPHA:314419
Ameloblastoma
Publications
10,254
Trials
6
Interventional, condition-specific
Researchers
1,077
Distinct authors in sample
Gene link
—
Readiness
2/6
Stages with a signal
Clinical definition (Orphanet)
A rare, benign, slow-growing odontologic tumor located in the mandible, and on occasion the maxilla, characterized by painless, variable-sized jaw swelling, which if left untreated may lead to a grotesque facial appearance. Occasionally, paresthesias, tooth displacement and adjacent root resorption may be associated. Local invasion is frequently observed, but malignant transformation and metastasis are not common.
How rare: How common this is has not been clearly measured.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0017795
- MeSH:D000564
- UMLS:C0002448
- NCIT:C4313
Additional Mondo synonyms (2)
ameloblastoma · ameloblastoma of jaw
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
10,254 matched papers (4,273 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
6 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?
10,254
10,254 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.
10,254 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).
4,273 in the last 10 years · low confidence
Phrase hits: 10,254 · MeSH hits: 324
Who's working on it?
1,077
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.
- 01Akintoye SO5 papers · 2026
Department of Oral Medicine, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA. akintoye@upenn.edu.
Papers in Europe PMC - 02Liu X5 papers · 2026
Orthopedic Department, Peking University Third Hospital, Beijing, China.
Papers in Europe PMC - 03Vargas PA5 papers · 2026
Oral Diagnosis Department, Piracicaba Dental School, Universidade Estadual de Campinas, Piracicaba, Brazil.
Papers in Europe PMC - 04Huang Y4 papers · 2026
Hospital of Stomatology, Sun Yat-Sen University, Guangzhou, 510055, China.
Papers in Europe PMC - 05Gao X3 papers · 2026
Department of Oral and Maxillofacial Surgery, Affiliated Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Papers in Europe PMC - 06Gomez RS3 papers · 2026
Department of Oral Pathology and Medicine, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil; Medical School, Faculdade Ciências Médicas de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Papers in Europe PMC - 07Li H3 papers · 2026
Department of Oral and Maxillofacial Surgery, Jinan Stomatological Hospital, Central Laboratory of Jinan Stomatological Hospital, Jinan Key Laboratory of Oral Tissue Regeneration, No. 101 Jingliu Street, Jinan, 250001 Shandong Province China.
Papers in Europe PMC - 08Li J3 papers · 2026
School of Electronic and Information Engineering, Beijing Jiaotong University, Beijing 100044, China.
Papers in Europe PMC - 09Li Y3 papers · 2026
Department of Stomatology, Hangzhou Stomatology Hospital, Hangzhou 310002, China.
Papers in Europe PMC - 10Li Z3 papers · 2026
Orthopedic Department, Peking University Third Hospital, Beijing, China.
Papers in Europe PMC
Clinical research
Is a treatment being tested?
6
interventional trials for this specific condition
6 interventional trials matched this specific condition name; 3 currently recruiting in our sample.
Data as of 27 July 2026
6 interventional trials — more than 73% of diseases in the trials denominator have none at all (5114 of 7003; this disease is at the 89th percentile).
low confidence · 89th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
6 interventional trials matched after quoted-phrase search and title/condition post-filter.
- NCT06653517·RECRUITING·Clinical Study of Neoadjuvant Targeted Therapy for Ameloblastoma
Conditions: Ameloblastoma · BRAF V600E Mutation Positive·Matched via name + MeSH
- NCT07306962·RECRUITING·Virtual Lesion Segmentation and Mandibular Ameloblastoma Radiographic Safety Margin
Conditions: Ameloblastoma·Matched via name + MeSH
- NCT06819605·NOT YET RECRUITING·Neoadjuvant Therapy With Conservative Surgery vs. Up-front Conservative Surgery for BRAF V600E-Mutated Ameloblastoma
Conditions: Ameloblastoma·Matched via name + MeSH
Observational and natural-history studies
1 observational study matches 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.
None of the matched observational studies is currently listed as recruiting.
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.
"Ameloblastoma" OR "ameloblastoma of jaw" OR "ameloblastoma of the jaw"
MeSH descriptor terms unioned into the query: Ameloblastoma
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Ameloblastoma" OR "ameloblastoma of jaw" OR "ameloblastoma of the jaw"
Interventional trials matched via: both (mesh = registered under a MeSH descriptor no name phrase would catch; recall-expansion = gene / selected parent terms used only for trials).
Study-type breakdown: 6 interventional · 1 observational · 0 expanded access. Only interventional studies enter the trial headline.
Query health: ok — strategies attempted: phrase, mesh; with hits: phrase, mesh
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 (10254) is extremely high with unknown/missing prevalence — treat as possible over-matching, not proven research intensity
Ingested 2026-07-27T13:06:38.530Z
