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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 | RareConnect | RareConnect.io

/Prader-Willi syndrome due to paternal 15q11q13 deletion

/Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2

Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2

Rare Disease

MONDO:0015784

Also Known As

Prader-Willi Syndrome (Type 2)

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External Resources

Orphanet

Orphanet:177904 ↗

GARD

Related Diseases

Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1

MONDO:0015783

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