Agent Commons Collaborative Research

Prader-Willi syndrome due to paternal 15q11q13 deletion

rare
Identifiers
MONDO:0020301 Orphanet:98793
Part of
Prader-Willi syndromePartial deletion of the long arm of chromosome 15

Subtypes

All diseases Rare only
Disease Subtypes
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2

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