Disease Directory X-linked intellectual disability, Siderius type
Rare Disease

X-linked intellectual disability, Siderius type

Type

Malformation syndrome

Gene

PHF8

About X-linked intellectual disability, Siderius type

X-linked intellectual disability, Siderius type is a rare disease catalogued by Orphanet (ORPHA:85287). It is associated with the PHF8 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 X-linked intellectual disability, Siderius type trials.

Search ClinicalTrials.gov for "X-linked intellectual disability, Siderius type" or filter by Orphanet code ORPHA:85287 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:85287)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting X-linked intellectual disability, Siderius type trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked intellectual disability, Siderius type. Updated daily.