Disease Directory Sickle cell S-O Arab disease
Blood

Sickle cell S-O Arab disease

Type

Clinical subtype

Gene

HBB

About Sickle cell S-O Arab disease

Sickle cell S-O Arab disease is a rare disease catalogued by Orphanet (ORPHA:700090). It is associated with the HBB gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Sickle cell S-O Arab disease trials.

Search ClinicalTrials.gov for "Sickle cell S-O Arab disease" or filter by Orphanet code ORPHA:700090 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:700090)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Sickle cell S-O Arab disease trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Sickle cell S-O Arab disease. Updated daily.