Disease Directory Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome
Rare Disease

Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome

Type

Malformation syndrome

Gene

ZBTB7A

About Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome

Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome is a rare disease catalogued by Orphanet (ORPHA:694956). It is associated with the ZBTB7A 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 Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome trials.

Search ClinicalTrials.gov for "Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome" or filter by Orphanet code ORPHA:694956 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:694956)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome. Updated daily.