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cataract-glaucoma syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

cataract-glaucoma syndrome

MONDO:0015567

Also known as:cataract - glaucoma

Overview

Cataract-glaucoma syndrome is characterized by the association of total bilateral congenital cataract with the secondary occurrence of glaucoma appearing at ages varying between 10 and 40 years.

Diagnosis

Biomarker and diagnostic research for cataract-glaucoma syndrome has been reported in the published literature.

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for cataract-glaucoma syndrome.

55 publications have been identified in PubMed for cataract-glaucoma syndrome. Research spans Epidemiology / Natural History (48%), Review / Meta-Analysis (25%), and Case Report / Case Series (13%).

Research Type	Count	% of Total
Disease patterns and progression	25	48%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:50 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:162

GARD

Genetic and Rare Diseases Info Center

GARD:1160

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
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cataract-glaucoma syndrome

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications