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17q11.2 microduplication syndrome

rare

17q11.2 microduplication syndrome is characterized by dysmorphic features and intellectual deficit.

Identifiers
MONDO:0015350 OMIM:618874Orphanet:139474
Part of
Hereditary diseasePartial duplication of the long arm of chromosome 17
Also known as
chromosome 17q11.2 duplication syndrome, 1.4-mb · dup(17)(q11.2) · Grisart-Destree syndrome · Grisart-Destrée syndrome · Nf1 Microduplication Syndrome

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