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cataract 37 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

cataract 37

MONDO:0013744

Also known as:CTRCT37cataract 37, autosomal dominantcataract type 37

Overview

A cataract that has material basis in variation in the region 12q24.2-q24.3.

GeneticsAutosomal dominant

Clinical Presentation

Features include: Developmental cataract.

Organ System	Phenotype Count	Example Features
Eyes	1	Developmental cataract

Explore clinical features

Diagnosis

Biomarker and diagnostic research for cataract 37 has been reported in the published literature.

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 37.

270 publications have been identified in PubMed for cataract 37. Research spans Clinical Trial Publication (34%), Epidemiology / Natural History (32%), and Review / Meta-Analysis (15%).

Research Type	Count	% of Total
Clinical study results	93	34%

Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 6:03 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:614422

GARD

Genetic and Rare Diseases Info Center

GARD:15800

Questions for Your Care Team

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cataract 37

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

Questions for Your Care Team

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