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ORPHA:611201

Oculogastrointestinal-neurodevelopmental syndrome

high confidenceDisorder

Also known as: OGIN Syndrome

Publications

141

59.9th percentile

Trials

0

Interventional, condition-specific

Researchers

51

Distinct authors in sample

Gene link

CAPN15

Strong

Readiness

3/6

Stages with a signal

Clinical definition (Orphanet)

A rare multiple anomalies/ syndrome characterized by eye abnormalities (including unilateral/bilateral microphthalmia, coloboma, unilateral ptosis and lens opacity) in addition to , renal anomalies (mainly horseshoe kidney, however ureteral-pelvic junction dysfunction and vesicoureteral reflux were also reported), imperforate anus and global . Majority of the patients also present with hearing impairment, cardiac anomalies and features (triangular face, hypoplastic alae nasi, beaked nose, and small pointed chin).

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.

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.”

3/6 stages with a signal

No matched interventional trial; the gene is known and literature exists — preclinical or natural-history work may still be the practical next step.

  1. Gene identifiedPresent

    Strong — CAPN15

  2. LiteraturePresent

    141 matched papers (122 in last 10 years) Source

  3. Phenotype characterisedPresent

    19 HPO annotations (e.g. Microcephaly; Anal atresia; Short stature) Source

  4. Animal modelNot found

    No Alliance genotype “model of” associations via Monarch for these Mondo IDs

  5. Orphan designationNot found

    No FDA or EMA orphan-drug designation matched this disease via UMLS or preferred name Source

  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?

Yes — we know a specific gene responsible (CAPN15).

GenCC classification: Strong.

Phenotypes (Monarch / HPO)

19

Associated phenotypes · MONDO:0036189

  • Microcephaly
  • Anal atresia
  • Short stature
  • Dysphonia
  • Autistic behavior

Showing 5 of 19 — open Monarch for the full list.

Animal models (Monarch / Alliance)

None returned for this Mondo ID. Empty here is not proof that no model organism work exists under another name or gene.

Monarch fetch 2026-07-29

Therapies

Designations, candidates, and chemicals

FDA OOPD and EMA orphan designations, Open Targets clinical candidates, and CTD chemical associations via MyDisease.info. These never change the interventional-trial headline.

Orphan designation (FDA · EMA)

No designation matched this disease via UMLS or preferred name on the FDA OOPD mirror or EMA orphan register. Absence here is not proof that none exists under another wording.

Open Targets candidates

No drugs or clinical candidates returned for this Mondo ID on Open Targets.

CTD chemicals (MyDisease.info)

No CTD chemical associations returned for this Mondo ID.

Literature

Is anyone studying this?

141

141 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=3967) is 59.

141 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 59 (publications denominator n=3967).

122 in the last 10 years · high confidence · 59.9th percentile (publications denominator)

Phrase hits: 6 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

51

Distinct author names in 6 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
    Cohen JL2 papers · 2023

    Duke University Department of Pediatrics, Division of Medical Genetics, Durham, NC 27710, USA.

    Papers in Europe PMC
  2. 02
    Hobbs CA2 papers · 2023

    Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, CA 92123, USA.

    Papers in Europe PMC
  3. 03
    Allegri L1 paper · 2024

    Department of Medicine (DMED), University of Udine, Udine, Italy.

    Papers in Europe PMC
  4. 04
    Baldan F1 paper · 2024

    Department of Medicine (DMED), University of Udine, Udine, Italy.

    Papers in Europe PMC
  5. 05
    Barrows C1 paper · 2023

    Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, California, USA.

    Papers in Europe PMC
  6. 06
    Beaman M1 paper · 2022

    Duke University Medical Scientist Training Program, Durham, NC 27710, USA.

    Papers in Europe PMC
  7. 07
    Beaman MM1 paper · 2023

    Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina, USA.

    Papers in Europe PMC
  8. 08
    Bregant E1 paper · 2024

    Institute of Medical Genetics, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), Udine, Italy.

    Papers in Europe PMC
  9. 09
    Chrestian N1 paper · 2025

    Department of Pediatric Neurology, Pediatric Neuromuscular Disorders, Centre Mère Enfant Soleil, Laval University, Quebec City, Quebec, Canada.

    Papers in Europe PMC
  10. 10
    Cocanougher BT1 paper · 2022

    Duke University Department of Pediatrics, Division of Medical Genetics, Durham, NC 27710, USA.

    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 11 September 2026 · last trial check 11 September 2026

No matched interventional trials. This is true for 77.2% of diseases in the trials denominator (5501 of 7126). Here are the researchers publishing on it.

high confidence · 38.6th 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.

Other registries (secondary)

Broader net from EU CTIS, ISRCTN, and ICTRP when available — deduped against ClinicalTrials.gov IDs already counted above. Dual-model LLM relevance gates what we keep. These rows are not added to the interventional headline.

raw 0 · after dedupe 0 · already on CT.gov 0 · kept 0 · parent 0 · uncertain 0 · dropped 0 · fetched 2026-07-30

Source notes: ictrp: Error: ICTRP public search unavailable (WHO portal is SPA-only; SOAP needs partnership). Tried: https://apps.who.int/tri

No secondary-registry studies passed dual-model relevance for this condition name (after dedupe).

Where to find support

Condition-specific patient organisations, when Orphanet lists them, are on the disease’s Orphanet page. We also link umbrella groups that support undiagnosed and ultra-rare families.

Orphanet entry for Oculogastrointestinal-neurodevelopmental syndrome — check Associations / patient organisations on that page.

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.

("Oculogastrointestinal-neurodevelopmental syndrome" OR "OGIN Syndrome") OR ("CAPN15" OR "CAPN15 syndrome" OR "CAPN15-related")

Run this search on Europe PMC

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

"Oculogastrointestinal-neurodevelopmental syndrome" OR "OGIN Syndrome"

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
  • No label/synonym collisions with other diseases in this corpus

Ingested 2026-07-27T19:02:24.003Z