RARE DISEASERESEARCH ATLAS

ORPHA:64692

Bartonella bacilliformis infection

medium confidenceDisorder

Also known as: Bartonellosis due to infection with Bartonella bacilliformis · Carrion disease

Publications

80

49.1th percentile

Trials

0

Interventional, condition-specific

Researchers

359

Distinct authors in sample

Gene link

Readiness

1/6

Stages with a signal

Clinical definition (Orphanet)

A rare bacterial infectious disease transmitted between humans via bites from infected sand flies in high-altitude valleys of the South American Andes, characterized by two disparate syndromes which can arise independently or sequentially. The first, Oroya fever, occurs about 60 days after the fly bite as a severe hemorrhagic fever with high mortality in untreated individuals. The second, chronic phase, termed verruga peruana, can persist for months or years and manifests with endothelial cell-derived, blood-filled tumors developing on the surface of the skin.

How rare: How common this is has not been clearly measured.

Orphanet entry

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.”

1/6 stages with a signal

Research-stage checklist from open sources (GenCC, literature, Monarch when enriched, ClinicalTrials.gov). Not a prognosis or care recommendation.

  1. Gene identifiedNot found

    No GenCC disease–gene assertion in this build

  2. LiteraturePresent

    80 matched papers (39 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 trialNot found

    No matched interventional trial under our ClinicalTrials.gov rules

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?

80

80 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.

80 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).

39 in the last 10 years · medium confidence · 49.1th percentile (publications denominator)

Phrase hits: 80 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

359

Distinct author names in 80 sampled papers — named people below.

Who's working on it?

No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.

  1. 01
    Noguchi H3 papers · 1929

    Laboratories of The Rockefeller Institute for Medical Research.

    Papers in Europe PMC
  2. 02
    Parola P3 papers · 2023

    Faculté des Sciences Médicales et Paramédicales, Aix Marseille Univ IRD, AP-HM, SSA, VITROME, 19-21 Boulevard Jean Moulin, 13005 Marseille, France.

    Papers in Europe PMC
  3. 03
    Angkasekwinai N2 papers · 2014

    Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America; Naval Medical Research Center, Silver Spring, Maryland, United States of America; Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

    Papers in Europe PMC
  4. 04
    Atkins EH2 papers · 2014

    Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America; Naval Medical Research Center, Silver Spring, Maryland, United States of America.

    Papers in Europe PMC
  5. 05
    Chao CC2 papers · 2014

    Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America; Naval Medical Research Center, Silver Spring, Maryland, United States of America.

    Papers in Europe PMC
  6. 06
    CHING Wei-Mei2 papers · 2007
    Papers in Europe PMC
  7. 07
    Ching WM2 papers · 2014

    Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America; Naval Medical Research Center, Silver Spring, Maryland, United States of America.

    Papers in Europe PMC
  8. 08
    Drummond MR2 papers · 2023

    Applied Research in Dermatology and Bartonella Infection Laboratory, University of Campinas-UNICAMP; Campinas, Sao Paulo, Brazil.

    Papers in Europe PMC
  9. 09
    Fenollar F2 papers · 2021

    Aix Marseille Univ, IRD, AP-HM, Microbes, VITROME, Marseille, France.

    Papers in Europe PMC
  10. 10
    HENDRIX Laura2 papers · 2007
    Papers in Europe PMC

Clinical research

Is a treatment being tested?

0

interventional trials for this specific condition

No interventional trial testing a treatment matched this specific condition name on ClinicalTrials.gov (observational studies and pan-disease registries are listed separately when present).

Data as of 27 July 2026

No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.

medium confidence · 36.5th percentile (trials denominator)

Recruiting interventional trials

From the matched ClinicalTrials.gov set

No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.

See who's working on it — people publishing on this disease are often the practical next contact when no trial is listed.

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.

"Bartonella bacilliformis infection" OR "Bartonellosis due to infection with Bartonella bacilliformis" OR "Carrion disease"

Run this search on Europe PMC

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

"Bartonella bacilliformis infection" OR "Bartonellosis due to infection with Bartonella bacilliformis" OR "Carrion disease"

Study-type breakdown: 0 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
  • "Carrion disease" also appears on ORPHA:659756

Ingested 2026-07-27T01:09:00.431Z