RARE DISEASERESEARCH ATLAS

ORPHA:54251

Aseptic abscess syndrome

high confidenceDisorder

Also known as: Aseptic abscesses syndrome · Aseptic systemic abscesses · Corticosteroid-sensitive aseptic abscess syndrome · Disseminated aseptic abscesses

Publications

75

56.2th percentile

Trials

1

Interventional, condition-specific

Researchers

468

Distinct authors in sample

Gene link

Readiness

2/6

Stages with a signal

Clinical definition (Orphanet)

A rare autoinflammatory disorder characterized by recurrent attacks of fever and sterile abscesses.

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 (3)

aseptic abscesses syndrome · aseptic systemic abscesses · disseminated aseptic abscesses

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.

  1. Gene identifiedNot found

    No GenCC disease–gene assertion in this build

  2. LiteraturePresent

    75 matched papers (58 in last 10 years) Source

  3. Phenotype characterisedNot checked

    Not yet enriched from Monarch / HPO

  4. Animal modelNot checked

    Not yet enriched from Monarch / Alliance

  5. Orphan designationNot checked

    FDA/EMA orphan-drug designation not enriched yet

  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)

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?

75

75 papers have ever been published on this condition (under this name). For scale, breast cancer has over 700,000. Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.

75 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).

58 in the last 10 years · high confidence · 56.2th percentile (publications denominator)

Phrase hits: 75 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

468

Distinct author names in 75 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
    Aumaître O5 papers · 2014
    Papers in Europe PMC
  2. 02
    Piette JC5 papers · 2022

    Service de Médecine Interne, AP-HP Groupe Hospitalier Pitié-Salpêtrière, 75013 Paris, France.

    Papers in Europe PMC
  3. 03
    Marzano AV4 papers · 2022

    Department of Pathophysiology and Transplantation, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Italy. angelovalerio.marzano@policlinico.mi.it

    Papers in Europe PMC
  4. 04
    André M3 papers · 2022

    Department of Internal Medicine, University Hospital Gabriel Montpied, Clermont-Ferrand, France.

    Papers in Europe PMC
  5. 05
    André MF3 papers · 2014

    Inserm, U931, GReD, Faculté de Médecine, Clermont-Ferrand, France. mandre@chu-clermontferrand.fr

    Papers in Europe PMC
  6. 06
    Grateau G3 papers · 2018

    Service de médecine interne, université Paris 6, Pierre-et-Marie-Curie (UPMC), hôpital Tenon, Assistance publique-Hôpitaux de Paris (AP-HP), 20, rue de la Chine, 75020 Paris, France; Inserm UMRS_933, université Pierre-et-Marie-Curie (UPMC)-Paris 6, hôpital Trousseau, Assistance publique-Hôpitaux de Paris, 75012 Paris, France; Centre de référence des maladies auto-inflammatoires et de l'amylose inflammatoire (CEREMAIA), 75020 Paris, France.

    Papers in Europe PMC
  7. 07
    Alaibac M2 papers · 2023

    Dermatology Unit, Department of Medicine, University of Padova, I-35128 Padova, Italy.

    Papers in Europe PMC
  8. 08
    Andre M2 papers · 2023

    Inserm U1071, M2iSH, USC-INRA 1382, Université Clermont Auvergne, Clermont-Ferrand, Auvergne-Rhône-Alpes, France.

    Papers in Europe PMC
  9. 09
    Aumaitre O2 papers · 2022

    Médecine Interne, CHU Gabriel Montpied, 63000 Clermont-Ferrand, France.

    Papers in Europe PMC
  10. 10
    Cardoso MC2 papers · 2010
    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 27 July 2026

1 interventional trial — more than 73% of diseases in the trials denominator have none at all (5114 of 7003; this disease is at the 76.8th percentile).

high confidence · 76.8th 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.

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 2026-07-26

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.

"Aseptic abscess syndrome" OR "Aseptic abscesses syndrome" OR "Aseptic systemic abscesses" OR "Corticosteroid-sensitive aseptic abscess syndrome" OR "Disseminated aseptic abscesses"

Run this search on Europe PMC

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

"Aseptic abscess syndrome" OR "Aseptic abscesses syndrome" OR "Aseptic systemic abscesses" OR "Corticosteroid-sensitive aseptic abscess syndrome" OR "Disseminated aseptic abscesses"

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 · 0 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 multi-word and distinctive
  • No synonyms dropped by stoplist
  • No label/synonym collisions with other diseases in this corpus

Ingested 2026-07-27T00:55:49.703Z