Dysspondyloenchondromatosis

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ORPHA:85198Q78.4
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8Treatment centers

Where are you in your journey?

UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Clinical phenotype terms— hover any for plain English:

Spondylometaphyseal dysplasiaHP:0002657Generalized joint hypermobilityHP:0002761AnisospondylyHP:0002879Enlarged jointsHP:0003037Abnormal ulnar metaphysis morphologyHP:0004039Multiple enchondromatosisHP:0005701Metaphyseal enchondromatosisHP:0005868Pretibial blisteringHP:0012221
Orphanet ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Dysspondyloenchondromatosis.

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No actively recruiting trials found for Dysspondyloenchondromatosis at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Dysspondyloenchondromatosis community →

No specialists are currently listed for Dysspondyloenchondromatosis.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Dysspondyloenchondromatosis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Dysspondyloenchondromatosis

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.