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cataract 8 multiple types - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

cataract 8 multiple types

MONDO:0007280

Also known as:CTRCT8cataract, congenital, Volkmann typecataract 8, multiple types

Overview

A cataract that has material basis in variation in the region 1pter-p36.13.

GeneticsAutosomal dominant

OnsetCONGENITAL

ResearchLimited published research (5 articles)

Clinical Presentation

Features include always present findings: Nuclear cataract. 3 total HPO annotations.

Organ System	Phenotype Count	Example Features
Eyes	2	Nuclear cataract, Developmental cataract

Age of onset: at birth.

Explore clinical features

Diagnosis

Biomarker and diagnostic research for cataract 8 multiple types has been reported in the published literature.

Prognosis

Phenotype severity distribution: 1 always present feature.

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 8 multiple types.

5 publications have been identified in PubMed for cataract 8 multiple types. Research spans Clinical Trial Publication (40%), Diagnostic / Biomarker (20%), and Review / Meta-Analysis (20%).

Recent Publications

Khalil MB (2026). [PMID: 42223495](https://pubmed.ncbi.nlm.nih.gov/42223495/). *Int Ophthalmol*. [Diagnostic / Biomarker]
Wang X (2025). [PMID: 41088899](https://pubmed.ncbi.nlm.nih.gov/41088899/). *Comb Chem High Throughput Screen*. [Epidemiology / Natural History]
Webster M (2025). [PMID: 39680667](https://pubmed.ncbi.nlm.nih.gov/39680667/). *J Cataract Refract Surg*. [Clinical Trial Publication]
Grad J (2025). [PMID: 39539848](https://pubmed.ncbi.nlm.nih.gov/39539848/). *J Vitreoretin Dis*. [Review / Meta-Analysis]
Lu SH (2025). [PMID: 40904306](https://pubmed.ncbi.nlm.nih.gov/40904306/). *Zhonghua Yi Xue Za Zhi*. [Clinical Trial Publication]

Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 12:48 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:115665

Orphanet

European rare disease database

Orphanet:98983

Questions for Your Care Team

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cataract 8 multiple types

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Orphanet

Related Diseases

Questions for Your Care Team

Questions for Your Care Team