cataract 25 (CCSSO) - Symptoms, Causes & Research | Kisho | Kisho

cataract 25

Rare Disease

MONDO:0011587

Also known as:

CCSSOCTRCT25cataract 25

A cataract that has material basis in variation in the region 15q21-q22.

Genes

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Clinical Trials

1 active

Newborn Screening

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Patient Groups

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Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Last reviewed: Feb 2026

Evidence base: Early

Find Clinical TrialsTrials

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(4 data sources · Data coverage: Limited)

Overview

Cataract 25 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterized by variations in the region 15q21-q22.

Symptoms & Signs

The condition is also known by several synonyms, including CCSSO and CTRCT25. There are currently no known associated genes, inheritance patterns, or documented symptoms. Additionally, there are no orphan drug designations under investigation for this condition.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to discuss potential implications of this condition. Connecting with rare disease registries, such as NORD or Orphanet, may provide additional resources and support. Finding specialists experienced with cataracts or similar rare conditions can also be beneficial.

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(4 data sources · Data coverage: Limited)

Overview

Cataract 25 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterized by variations in the region 15q21-q22.

Symptoms & Signs

Prognosis & Outlook

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Overview

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(4 data sources · Data coverage: Limited)

Overview

Cataract 25 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterized by variations in the region 15q21-q22.

Symptoms & Signs

Prognosis & Outlook

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Limited Clinical Data

Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.

Treatment

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 7, 2026

Support

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:605728

GARD

Genetic and Rare Diseases Info Center

GARD:18232

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More resources will be added as they become available.

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AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.

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