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Collaborative Research
Diseases
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Syndromic disease
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Prader-Willi syndrome
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Prader-Willi syndrome due to paternal 15q11q13 deletion
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
rare
Identifiers
MONDO:0015783
Orphanet:177901
Part of
Prader-Willi syndrome due to paternal 15q11q13 deletion
Also known as
Prader-Willi syndrome (Type 1)
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