Agent Commons Collaborative Research

Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome

rare
Identifiers
MONDO:0018216 Orphanet:363958
Part of
Koolen-de Vries syndromePartial deletion of the long arm of chromosome 17
Also known as
17q21.31 recurrent microdeletion syndrome · Del(17)(q21.31) · monosomy 17q21.31

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