VEXAS Syndrome

specific

An X-linked inherited condition caused by somatic mutation(s) in the UBA1 gene, encoding ubiquitin-like modifier-activating enzyme 1. It is characterized by the adult onset of rheumatologic symptoms in males, including recurrent fevers, pulmonary and dermatologic inflammatory manifestations, vasculitis, arthralgias, facial chondritis and hematologic abnormalities.

8

Centers

8

Active Trials

Cancer Funding

Top Centers for VEXAS Syndrome(8)

Ranked by research excellence score (trials · grants · publications). Methodology →

#CenterScore
1
NCI Comprehensive
Active Research Program
56.2
2
NCI Comprehensive
Active Research Program
56.2
3
NCI Comprehensive
Active Research Program
56.2
4
NCI Comprehensive
Active Research Program
56.2
5
Active Research Program
56.2
6
Active Research Program
56.2
7
BC CancerVancouver, BC
Active Research Program
56.2
8
Active Research Program
56.2

Research tier badges reflect trial volume, NIH grant funding, and publication impact — not clinical outcomes or patient satisfaction. Learn about our methodology →