Disease Directory Intermediate osteopetrosis
Rare Disease

Intermediate osteopetrosis

Type

Malformation syndrome

Gene

TCIRG1, CLCN7, PLEKHM1

About Intermediate osteopetrosis

Intermediate osteopetrosis is a rare disease catalogued by Orphanet (ORPHA:210110). It is associated with the TCIRG1, CLCN7, PLEKHM1 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 Intermediate osteopetrosis trials.

Search ClinicalTrials.gov for "Intermediate osteopetrosis" or filter by Orphanet code ORPHA:210110 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:210110)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Intermediate osteopetrosis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Intermediate osteopetrosis. Updated daily.