Tatton Brown Rahman Syndrome (TBRS) is a rare genetic condition caused by mutations in the DNMT3A gene. The TBRS Community is dedicated to supporting families affected by this syndrome, advancing research, and building a network of connections among patients, families, clinicians, and researchers.
2017
81-2216511
$832.9 thousand
This organization contributes to the following United Nations Sustainable Development Goals. See the SDG page for more information.
An informational resource designed to support newly diagnosed families.
A conference that brings researchers and clinicians together to discuss TBRS and related research.
An event that unites the TBRS community for networking and sharing experiences.
October 7, 2022
The 2022 TBRS Community Virtual Family Conference featured talks from prominent clinicians and researchers about TBRS.
September 20, 2022
The TBRS Collaborative Research Network Conference brought together experts to discuss ongoing research related to TBRS.
February 28, 2024
Quarterly virtual meet-ups for newly diagnosed and existing TBRS families to connect and share experiences.
Learn MoreAugust 7, 2023
Bringing together the community for the first time since 2011 with a Family Conference.
Learn MoreOverall Score
46
50
/100
Program Expense Ratio
72.78%
8
/20
Program Revenue Growth
-100.00%
2
/20
Leverage Ratio
0.0104
20
/20
Working Capital Ratio
5.247
18
/20
Fundraising Efficiency
0
2
/20
Fiscal Year:2022
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 163.6K | 98.93% |
Program Services | 0 | 0.00% |
Investment Income | 0 | 0.00% |
Sales of Non-Inventory Assets | 0 | 0.00% |
Other Notable Sources | 1.768K | 1.07% |
Total Revenue | 165.4K | 100.00% |
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