RARE DISEASERESEARCH ATLAS

ORPHA:714164

Acute posterior multifocal placoid pigment epitheliopathy

low confidence

Also known as: APMPPE

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

Orphanet entry

Is anyone studying this?

814

814 papers have been published on this condition. That is a real research literature — still far smaller than common diseases (breast cancer: over 700,000 papers). Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=183) is 38.

814 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 38 (publications denominator n=183).

464 in the last 10 years · low confidence

Is a treatment being tested?

0

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 26 July 2026

No matched interventional trials. This is true for 59.2% of diseases in the trials denominator (151 of 255). Here are the researchers publishing on it.

low confidence · 29.6th percentile (trials denominator)

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.

Who's working on it?

869

Distinct author names in 200 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
    Herbort CP Jr11 papers · 2026

    Retinal and Inflammatory Eye Diseases, Centre for Ophthalmic Specialized Care (COS), 1003 Lausanne, Switzerland.

    Papers in Europe PMC
  2. 02
    Papasavvas I11 papers · 2026

    Retinal and Inflammatory Eye Diseases, Centre for Ophthalmic Specialized Care (COS), 1003 Lausanne, Switzerland.

    Papers in Europe PMC
  3. 03
    Sarraf D7 papers · 2026

    Stein Eye Institute, University of California-Los Angeles School of Medicine, Los Angeles, USA.

    Papers in Europe PMC
  4. 04
    Agarwal A5 papers · 2026

    The Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.

    Papers in Europe PMC
  5. 05
    Gupta V5 papers · 2026

    Advanced Eye Centre (V.G.), Postgraduate Institute of Medical Education and Research, Chandigarh, India. Electronic address: vishalisara@gmail.com.

    Papers in Europe PMC
  6. 06
    Iwata D5 papers · 2023

    Department of Ophthalmology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, N-15, W-7, Kita-Ku, Sapporo, 060-8638, Japan.

    Papers in Europe PMC
  7. 07
    Mantovani A5 papers · 2024

    Department of Ophthalmology, Ospedale Valduce, Como, Italy.

    Papers in Europe PMC
  8. 08
    Suzuki K5 papers · 2025

    Department of Ophthalmology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, N-15, W-7, Kita-Ku, Sapporo, 060-8638, Japan.

    Papers in Europe PMC
  9. 09
    Takeuchi M5 papers · 2026

    Department of Ophthalmology, National Defense Medical College, Saitama, Japan.

    Papers in Europe PMC
  10. 10
    Usui Y5 papers · 2026

    Department of Ophthalmology, Tokyo Medical University Hospital, Tokyo, Japan.

    Papers in Europe PMC

Recruiting interventional trials

Trials testing a treatment 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 above — 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 below but are not added to the query string.

"Acute posterior multifocal placoid pigment epitheliopathy" OR "APMPPE"

Run this search on Europe PMC

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

"Acute posterior multifocal placoid pigment epitheliopathy" OR "APMPPE"

Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.

0

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
  • No Orphanet definition and no Mondo IDs — likely taxonomy scaffolding; confidence capped at low

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