Disease Directory Autosomal thrombocytopenia with normal platelets
Blood

Autosomal thrombocytopenia with normal platelets

Type

Etiological subtype

Gene

IKZF5, ETV6, MASTL, CYCS, ANKRD26

About Autosomal thrombocytopenia with normal platelets

Autosomal thrombocytopenia with normal platelets is a rare disease catalogued by Orphanet (ORPHA:168629). It is associated with the IKZF5, ETV6, MASTL genes. 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 Autosomal thrombocytopenia with normal platelets trials.

Search ClinicalTrials.gov for "Autosomal thrombocytopenia with normal platelets" or filter by Orphanet code ORPHA:168629 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

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Orphanet

European reference resource for rare diseases (ORPHA:168629)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Autosomal thrombocytopenia with normal platelets trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal thrombocytopenia with normal platelets. Updated daily.