The Hidradenitis suppurativa Registry is an observational web-based registry for prospective anonymized collection of clinical data in individuals suffering from Hidradenitis suppurativa (HS). The website provides the information about HS as a disease, HS registry, research protocol, objectives, methods, recruitment and course of study. It offers various templates for doctors and patients to use as well as information on apps for HS. It provides a number of useful links and a collaboration form for Centers that wish to take part.
