ORPHA:98962
Granular corneal dystrophy type I
Also known as: Classic GCD · Classic granular corneal dystrophy · Corneal dystrophy Groenouw type I · GCD1 · GCDI · Granular corneal dystrophy type 1
Publications
113
55th percentile
Trials
1
Interventional, condition-specific
Researchers
588
Distinct authors in sample
Gene link
TGFBI
Definitive
Readiness
3/6
Stages with a signal
Clinical definition (Orphanet)
Type I granular corneal (GCDI) is a rare form of stromal corneal characterized by multiple small deposits in the superficial central corneal stroma, and visual impairment, which may sometimes be severe.
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:0007377
- MeSH:C537304
- OMIM:121900
- UMLS:C1641846
Additional Mondo synonyms (4)
classic GCD · classic granular corneal dystrophy · corneal dystrophy Groenouw type I · granular corneal dystrophy type 1
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
An interventional trial matched this condition name on ClinicalTrials.gov — see trials below.
- Gene identifiedPresent
Definitive — TGFBI
- LiteraturePresent
113 matched papers (55 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
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?
Yes — we know a specific gene responsible (TGFBI).
GenCC classification: Definitive.
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?
113
113 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.
113 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).
55 in the last 10 years · medium confidence · 55th percentile (publications denominator)
Phrase hits: 112 · MeSH hits: 1
Who's working on it?
588
Distinct author names in 113 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.
- 01Møller HU12 papers · 2024
Department of Ophthalmology, University Hospital, Arhus, Denmark.
Papers in Europe PMC - 02Kim EK6 papers · 2025
Department of Ophthalmology, Corneal Dystrophy Research Institute, Yonsei University College of Medicine, Seoul, South Korea.
Papers in Europe PMC - 03Klintworth GK6 papers · 2014
Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710, USA. klint001@mc.duke.edu
Papers in Europe PMC - 04Enghild JJ4 papers · 2015
Department of Molecular Biology and Genetics, Science Park, Aarhus University, Aarhus, Denmark 3Interdisciplinary Nanoscience Center (iNANO) and Center for Insoluble Protein Structures (inSPIN), Aarhus University, Aarhus, Denmark.
Papers in Europe PMC - 05Munier FL4 papers · 2024
Jules-Gonin Eye Hospital, University of Lausanne , Lausanne , Switzerland.
Papers in Europe PMC - 06Aldave AJ3 papers · 2017
From the Beijing Tongren Eye Center (Song, Sun, N. Wang, Zhang), Beijing Tongren Hospital, Capital Medical University and Beijing Ophthalmology & Visual Sciences Key Laboratory, the Peking University Third Hospital (Y. Chen), Beijing, Key Laboratory of Myopia, Ministry of Health, Department of Ophthalmology (Zhou, Zhao), the Eye and ENT Hospital of Fudan University, Shanghai, the Eye Hospital of Wenzhou Medical University (Q. Wang, S. Chen), Wenzhou, the West China Hospital of Sichuan University (Deng, Qiu), Chengdu, China; the Stein Eye Institute (Aldave), University of California Los Angeles Medical Center, Los Angeles, California, USA.
Papers in Europe PMC - 07Bozkurt B3 papers · 2026
Selçuk University Faculty of Medicine, Department of Ophtalmology, Konya, Turkey.
Papers in Europe PMC - 08Chao-Shern C3 papers · 2019
Biomedical Sciences Research Institute, University of Ulster, Coleraine, Northern Ireland, UK.
Papers in Europe PMC - 09Li M3 papers · 2023
Henan Eye Hospital, Henan Eye Institution, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, Henan, China.
Papers in Europe PMC - 10Lisch W3 papers · 2024
Department of Ophthalmology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany (Dr W. Lisch, Dr Wasielica-Poslednik); the Department of Ophthalmology, Helsinki University Central Hospital, Helsinki, Finland (Dr Kivelä); the Department of Ophthalmology, University of Erlangen-Nürnberg, Erlangen, Germany (Dr Schlötzer-Schrehardt); the Department of Ophthalmology, Eberhard-Karls University of Tübingen, Tübingen, Germany (Dr Rohrbach); the Department of Ophthalmology, University of Marburg, Marburg, Germany (Dr Sekundo); the Department of Ophthalmology, Campus Virchow-Klinikum, Charité Universitaetsmedizin Berlin, Berlin, Germany (Dr Pleyer); the private practice of ophthalmology Hanau, Hanau, Germany (Dr C. Lisch); the Department of Internal Medicine III, Johannes Gutenberg University Mainz, Mainz, Germany (Dr Desuki); the Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center Mainz, Mainz, Germany (Dr Rossmann); and the Department of Ophthalmology, Louisiana State University Health Sciences Center, School of Medicine, New Orleans, Louisiana (Dr Weiss).
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. 36 trials are registered for corneal dystrophy, the broader category — shown separately because they may or may not enrol this specific subtype.
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).
medium 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.
Broader category: corneal dystrophy
36
Interventional trials for the parent category, exclusive of NCT IDs already counted above. Eligibility for this subtype is not guaranteed.
Worth raising with a clinician. How we count trials.
Recruiting under the broader category
- NCT04440280·RECRUITING·Targeting Reactive Oxygen Species Production as a Novel Therapeutic in Fuch's Endothelial Corneal Dystrophy
Conditions: Fuchs Endothelial Corneal Dystrophy·Matched via name phrase
- NCT06425666·RECRUITING·Trial Comparing Cataract Surgery With Triple-DMEK in Patients With Cataract and Fuchs Endothelial Corneal Dystrophy
Conditions: Cataract Surgery · Cataract and Fuchs Endothelial Corneal Dystrophy·Matched via name phrase
- NCT07539012·RECRUITING·Effect of Descemet Membrane Polishing in Fuchs Endothelial Corneal Dystrophy
Conditions: Fuchs Endothelial Corneal Dystrophy·Matched via name phrase
- NCT07217249·ENROLLING BY INVITATION·Effect of Donor Diabetes and Other Factors on Corneal Transplant Endothelial Cell Loss and Success at 5 Years
Conditions: Fuchs Endothelial Corneal Dystrophy · Corneal Endothelial Decompensation·Matched via name phrase
- NCT07024693·RECRUITING·DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy
Conditions: Fuchs Endothelial Corneal Dystrophy · Fuchs·Matched via name phrase
- NCT04129021·RECRUITING·High Resolution, High-speed Multimodal Ophthalmic Imaging
Conditions: Retinitis Pigmentosa · Maculopathy, Age Related · Macular Dystrophy · Macular Edema·Matched via name phrase
- NCT07441616·NOT YET RECRUITING·Partial Range Of Field IOLs in DMEK-Enabled Procedures
Conditions: Cataract · Fuchs Endothelial Corneal Dystrophy·Matched via name phrase
- NCT07373821·RECRUITING·Influence of Supine Positioning on the Outcomes After Descemet Membrane Endothelial Keratoplasty (DMEK)
Conditions: Fuchs Endothelial Corneal Dystrophy · Descemet Membrane Endothelial Keratoplasty (DMEK)·Matched via name phrase
- NCT06844123·RECRUITING·Microsurgical Robot-assisted Corneal Transplant
Conditions: Corneal Dystrophy·Matched via name phrase
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.
"Granular corneal dystrophy type I" OR "Classic GCD" OR "Classic granular corneal dystrophy" OR "Corneal dystrophy Groenouw type I" OR "Granular corneal dystrophy type 1"
MeSH descriptor terms unioned into the query: Groenouw type I corneal dystrophy
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Granular corneal dystrophy type I" OR "Classic GCD" OR "Classic granular corneal dystrophy" OR "Corneal dystrophy Groenouw type I" OR "Granular corneal dystrophy type 1" OR "Groenouw type I corneal dystrophy" OR "TGFBI"
Recall-expansion terms: TGFBI
Interventional trials matched via: recall-expansion (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 · 1 observational · 0 expanded access. Only interventional studies enter the trial headline.
Parent-category trials query:
"corneal dystrophy"
Query health: ok — strategies attempted: phrase, mesh, recall-expansion; with hits: phrase, mesh, recall-expansion
Run this search on ClinicalTrials.gov
Synonyms dropped by stoplist: GCD1; GCDI
Confidence reasoning
- Preferred label is multi-word and distinctive
- 2 synonym(s) dropped by stoplist (may under-count)
- No label/synonym collisions with other diseases in this corpus
Ingested 2026-07-27T05:48:09.802Z
