Steroid-induced glaucoma
diseaseOn this page
Also known as corticosteroid-induced glaucoma
Summary
Steroid-induced glaucoma (MONDO:0004930) is a disease and 4 clinical trials. Top therapeutic interventions include dexamethasone. A subtype of glaucoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 4
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | steroid-induced glaucoma |
| Mondo ID | MONDO:0004930 |
| DOID | DOID:9946 |
| SNOMED CT | 1654001 |
| UMLS | C0339578 |
| MedGen | 573238 |
| Is cancer (heuristic) | no |
Also known as: corticosteroid-induced glaucoma
Disease family
This is a subtype of glaucoma. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › disorder of orbital region › eye disorder › glaucoma › steroid-induced glaucoma
Related subtypes (10): glaucomatous atrophy of optic disk, hypersecretion glaucoma, aqueous misdirection, phacogenic glaucoma, traumatic glaucoma, angle-closure glaucoma, borderline glaucoma, open-angle glaucoma, hereditary glaucoma, secondary early-onset glaucoma
Subtypes (1): residual stage corticosteroid-induced glaucoma
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 4.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 2 |
| PHASE4 | 1 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04075227 | PHASE4 | COMPLETED | Topical 0.2% Loteprednol Etabonate vs. Topical 0.1% Dexamethasone in Impending Recurrent Pterygium |
| NCT01912638 | PHASE1/PHASE2 | COMPLETED | Trabeculectomy With Ologen Collagen Implant vs Trabeculectomy With Provisc in Steroid Induced Glaucoma |
| NCT04593745 | Not specified | UNKNOWN | Intraocular Pressure in Children With Acute Lymphoblastic Leukemia (ALL) Treated With High Dose Steroids |
| NCT04673201 | Not specified | UNKNOWN | Management Steroid Induced Glaucoma |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| DEXAMETHASONE | 4 | 1 |
Related Atlas pages
- Drugs: Dexamethasone