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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1 | RareConnect | RareConnect.io

/Prader-Willi syndrome due to paternal 15q11q13 deletion

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

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

Rare Disease

MONDO:0015783

Also Known As

Prader-Willi syndrome (Type 1)

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External Resources

Orphanet

Orphanet:177901 ↗

GARD

Related Diseases

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

MONDO:0015784

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