Overview

This report reflects available clinical information. Some areas may remain under active research.(5 data sources · Data coverage: Moderate)

Overview

Galloway-Mowat syndrome 5 (GAMOS5) is a rare condition that has been recognized in scientific databases with the identifier OMIM:617731. While detailed descriptions about the condition are not available, it is known that research has identified a relationship with changes in the TPRKB gene. Because the available trusted sources provide limited descriptive information, understanding of the full clinical picture remains incomplete. More research is needed to clarify the characteristics and impacts of this condition on affected individuals.

Symptoms & Signs

Information about symptoms is currently limited for this condition.

Causes & Risk Factors

Galloway-Mowat syndrome 5 is linked to genetic variations in the TPRKB gene. However, information about additional genetic factors or environmental risks is currently limited.

Treatment & Management

Information about treatment is currently limited for this condition.

Prognosis & Outlook

Information about prognosis is currently limited for this condition.

Research & Clinical Trials

Information about current research and future directions is currently limited for this condition.

Quick Resources

Helpful links for rare disease information and support

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

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?
•Should my family members consider genetic testing?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Associated Genes

1 gene

TPRKB

Gene data from HGNC • Click to view on NCBI Gene

Inheritance Pattern

Autosomal Recessive

Inheritance patterns describe how genetic conditions are passed from parents to children.

Treatment

Support

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:617731

GARD

Genetic and Rare Diseases Info Center

GARD:16249

Know a Patient Advocacy Group for this condition?

Help patients and families find support by registering your organization or suggesting a group that serves this community.

Galloway-Mowat syndrome 5

Patient-Friendly Information

Associated Genes

Inheritance Pattern

Associated Genes

Inheritance Pattern

Overview

Overview

Symptoms & Signs

Causes & Risk Factors

Treatment & Management

Prognosis & Outlook

Research & Clinical Trials

Quick Resources

General Questions to Consider

Clinical

Associated Genes

Inheritance Pattern

Treatment

Support

External Resources

OMIM

GARD

Know a Patient Advocacy Group for this condition?

Need this data in your product?

Galloway-Mowat syndrome 5

Patient-Friendly Information

Associated Genes

Inheritance Pattern

Associated Genes

Inheritance Pattern

Overview

Overview

Symptoms & Signs

Causes & Risk Factors

Treatment & Management

Prognosis & Outlook

Research & Clinical Trials

Quick Resources

General Questions to Consider

Clinical

Associated Genes

Inheritance Pattern

Treatment

Support

External Resources

OMIM

GARD

Related Diseases

Know a Patient Advocacy Group for this condition?

Need this data in your product?