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Phelan-McDermid syndrome due to SHANK3 mutation | RareConnect | RareConnect.io

/Phelan-McDermid syndrome

/Phelan-McDermid syndrome due to SHANK3 mutation

Phelan-McDermid syndrome due to SHANK3 mutation

Rare Disease

MONDO:0971069

Patient-Friendly Information

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Patient Advocacy Groups

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P

Phelan-McDermid Syndrome Foundation

Primary Focus

RDCP:PAG0000180US

Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.

External Resources

Orphanet

Orphanet:662172 ↗

Related Diseases

Phelan-McDermid syndrome due to 22q13.3 deletion

MONDO:0971068

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