REGISTRY
ENROLL FOR A CAUSE
The TANGO2 Research has partnered with the Foundation Coordination of Rare Diseases at Sanford (CoRDS) to house patient registry data. CoRDS is a centralized international patient registry for rare diseases. The CoRDS registry allows patients and families to share important information about TANGO2 deficiency disorder with the people who can best use it, researchers! The data you provide is strictly confidential. Your privacy is the highest priority. You participation will allow us to better understand TANGO2 deficiency disorder, help drive research and find a cure!
Go to CoRDS Registry Now
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